Canonical Allele Identifier: CA375309076

Gene: POMT1

Linked Data

• MyVariant Identifiers: chr9:g.134388676T>C (hg19) ; chr9:g.131513289T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131513289T>C , CM000671.2:g.131513289T>C	GRCh38
NC_000009.11:g.134388676T>C , CM000671.1:g.134388676T>C	GRCh37
NC_000009.10:g.133378497T>C	NCBI36
NG_008896.1:g.15388T>C
NG_008896.2:g.15388T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000341012.13:c.971T>C	ENSP00000343034.7:p.Met324Thr
ENST00000404875.7:n.1673T>C
ENST00000423007.6:c.1190T>C	ENSP00000404119.2:p.Met397Thr
ENST00000677295.2:c.*1477T>C	ENSP00000504346.2:n.*1477T>C
ENST00000678264.2:c.*1316T>C	ENSP00000503157.2:n.*1316T>C
ENST00000682070.1:n.1598T>C
ENST00000682813.1:n.1398T>C
ENST00000683392.1:n.3880T>C
ENST00000683712.1:n.1538T>C
ENST00000683900.1:n.3033T>C
ENST00000684062.1:n.1799T>C
ENST00000684579.1:n.2979T>C
ENST00000341012.12:c.971T>C	ENSP00000343034.7:p.Met324Thr
ENST00000372220.5:c.2T>C	ENSP00000361294.5:p.Met1Thr
ENST00000372228.9:c.1199T>C	ENSP00000361302.3:p.Met400Thr
ENST00000402686.8:c.1133T>C MANE Select	ENSP00000385797.4:p.Met378Thr
ENST00000676640.1:c.1133T>C	ENSP00000503281.1:p.Met378Thr
ENST00000676803.1:c.308T>C	ENSP00000503093.1:p.Met103Thr
ENST00000676835.1:c.*348T>C	ENSP00000502911.1:n.*348T>C
ENST00000677029.1:c.677T>C	ENSP00000502936.1:p.Met226Thr
ENST00000677099.1:c.*843T>C	ENSP00000504553.1:n.*843T>C
ENST00000677216.1:c.782T>C	ENSP00000503772.1:p.Met261Thr
ENST00000677293.1:c.308T>C	ENSP00000504278.1:p.Met103Thr
ENST00000677295.1:c.*510T>C	ENSP00000504346.1:n.*510T>C
ENST00000677444.1:c.939T>C
ENST00000677586.1:n.614T>C
ENST00000677626.1:c.824+1822T>C	ENSP00000503552.1:n.824+1822T>C
ENST00000677677.1:n.1093T>C
ENST00000677853.1:c.*141T>C	ENSP00000503488.1:n.*141T>C
ENST00000677944.1:c.395T>C
ENST00000678264.1:c.*510T>C	ENSP00000503157.1:n.*510T>C
ENST00000678303.1:c.1043T>C	ENSP00000503696.1:p.Met348Thr
ENST00000678366.1:c.*1382T>C	ENSP00000504353.1:n.*1382T>C
ENST00000678546.1:c.*1078T>C	ENSP00000503062.1:n.*1078T>C
ENST00000678548.1:c.*1205T>C	ENSP00000503934.1:n.*1205T>C
ENST00000678626.1:n.830T>C
ENST00000678733.1:c.256+1153T>C
ENST00000678739.1:c.*1459T>C	ENSP00000503806.1:n.*1459T>C
ENST00000678795.1:n.220T>C
ENST00000678833.1:c.*580T>C	ENSP00000503893.1:n.*580T>C
ENST00000678942.1:c.313T>C	ENSP00000504690.1:n.313T>C
ENST00000679023.1:c.971T>C	ENSP00000503718.1:p.Met324Thr
ENST00000679073.1:c.511T>C	ENSP00000504356.1:n.511T>C
ENST00000679076.1:c.752T>C
ENST00000679111.1:c.1133T>C	ENSP00000504257.1:p.Met378Thr
ENST00000679189.1:c.782T>C	ENSP00000503356.1:p.Met261Thr
ENST00000341012.11:c.971T>C	ENSP00000343034.7:p.Met324Thr
ENST00000372228.7:c.1199T>C	ENSP00000361302.3:p.Met400Thr
ENST00000402686.7:c.1133T>C	ENSP00000385797.3:p.Met378Thr
ENST00000404875.6:c.782T>C	ENSP00000384531.2:p.Met261Thr
ENST00000423007.5:c.1133T>C	ENSP00000404119.1:p.Met378Thr
ENST00000441334.5:c.848T>C	ENSP00000395060.1:p.Met283Thr
ENST00000462375.5:n.959T>C
ENST00000485278.5:n.1688T>C
NM_001077365.1:c.1133T>C	NP_001070833.1:p.Met378Thr
NM_001077366.1:c.971T>C	NP_001070834.1:p.Met324Thr
NM_001136113.1:c.1133T>C	NP_001129585.1:p.Met378Thr
NM_001136114.1:c.782T>C	NP_001129586.1:p.Met261Thr
NM_007171.3:c.1199T>C	NP_009102.3:p.Met400Thr
XM_005272156.1:c.1199T>C	XP_005272213.1:p.Met400Thr
XM_005272158.1:c.1037T>C	XP_005272215.1:p.Met346Thr
XM_005272159.1:c.848T>C	XP_005272216.1:p.Met283Thr
XM_005272162.1:c.2T>C	XP_005272219.1:p.Met1Thr
XM_006716932.1:c.848T>C	XP_006716995.1:p.Met283Thr
XM_011518140.1:c.1052T>C	XP_011516442.1:p.Met351Thr
XM_011518141.1:c.986T>C	XP_011516443.1:p.Met329Thr
XM_011518142.1:c.890T>C	XP_011516444.1:p.Met297Thr
XM_011518143.1:c.884T>C	XP_011516445.1:p.Met295Thr
XM_011518144.1:c.1199T>C	XP_011516446.1:p.Met400Thr
XM_011518145.1:c.743T>C	XP_011516447.1:p.Met248Thr
XM_011518146.1:c.884T>C	XP_011516448.1:p.Met295Thr
XR_929703.1:n.1375T>C
NM_001353193.1:c.1199T>C	NP_001340122.1:p.Met400Thr
NM_001353194.1:c.971T>C	NP_001340123.1:p.Met324Thr
NM_001353195.1:c.782T>C	NP_001340124.1:p.Met261Thr
NM_001353196.1:c.1043T>C	NP_001340125.1:p.Met348Thr
NM_001353197.1:c.1037T>C	NP_001340126.1:p.Met346Thr
NM_001353198.1:c.1037T>C	NP_001340127.1:p.Met346Thr
NM_001353199.1:c.848T>C	NP_001340128.1:p.Met283Thr
NM_001353200.1:c.677T>C	NP_001340129.1:p.Met226Thr
NR_148391.1:n.1183T>C
NR_148392.1:n.1401T>C
NR_148393.1:n.1183T>C
NR_148394.1:n.1076T>C
NR_148395.1:n.1335T>C
NR_148396.1:n.969T>C
NR_148397.1:n.1233T>C
NR_148398.1:n.1188T>C
NR_148399.1:n.1575T>C
NR_148400.1:n.1174T>C
XM_005272162.3:c.2T>C	XP_005272219.1:p.Met1Thr
XM_006716932.2:c.848T>C	XP_006716995.1:p.Met283Thr
XM_011518140.2:c.1052T>C	XP_011516442.1:p.Met351Thr
XM_011518141.2:c.986T>C	XP_011516443.1:p.Met329Thr
XM_011518142.2:c.890T>C	XP_011516444.1:p.Met297Thr
XM_011518143.2:c.884T>C	XP_011516445.1:p.Met295Thr
XM_011518145.2:c.743T>C	XP_011516447.1:p.Met248Thr
XM_017014205.2:c.2T>C	XP_016869694.1:p.Met1Thr
XM_024447380.1:c.2T>C	XP_024303148.1:p.Met1Thr
XM_024447381.1:c.308T>C	XP_024303149.1:p.Met103Thr
XM_024447382.1:c.2T>C	XP_024303150.1:p.Met1Thr
XR_001746160.2:n.1303T>C
XR_001746162.2:n.1369T>C
XR_001746164.1:n.1086T>C
XR_001746166.2:n.1520T>C
NM_001077365.2:c.1133T>C MANE Select	NP_001070833.1:p.Met378Thr
NM_001077366.2:c.971T>C	NP_001070834.1:p.Met324Thr
NM_001136113.2:c.1133T>C	NP_001129585.1:p.Met378Thr
NM_001136114.2:c.782T>C	NP_001129586.1:p.Met261Thr
NM_001353193.2:c.1199T>C	NP_001340122.2:p.Met400Thr
NM_001353194.2:c.971T>C	NP_001340123.1:p.Met324Thr
NM_001353195.2:c.782T>C	NP_001340124.1:p.Met261Thr
NM_001353196.2:c.1043T>C	NP_001340125.1:p.Met348Thr
NM_001353197.2:c.1037T>C	NP_001340126.2:p.Met346Thr
NM_001353198.2:c.1037T>C	NP_001340127.2:p.Met346Thr
NM_001353199.2:c.848T>C	NP_001340128.2:p.Met283Thr
NM_001353200.2:c.677T>C	NP_001340129.1:p.Met226Thr
NM_001374689.1:c.1121T>C	NP_001361618.1:p.Met374Thr
NM_001374690.1:c.1133T>C	NP_001361619.1:p.Met378Thr
NM_001374691.1:c.782T>C	NP_001361620.1:p.Met261Thr
NM_001374692.1:c.782T>C	NP_001361621.1:p.Met261Thr
NM_001374693.1:c.824+1822T>C	NP_001361622.1:n.824+1822T>C
NM_001374695.1:c.743T>C	NP_001361624.1:p.Met248Thr
NM_007171.4:c.1199T>C	NP_009102.4:p.Met400Thr
NR_148391.2:n.1167T>C
NR_148392.2:n.1385T>C
NR_148393.2:n.1167T>C
NR_148394.2:n.1060T>C
NR_148395.2:n.1319T>C
NR_148396.2:n.953T>C
NR_148397.2:n.1217T>C
NR_148398.2:n.1172T>C
NR_148399.2:n.1559T>C
NR_148400.2:n.1158T>C