Canonical Allele Identifier: CA200798927

Gene: POMT1

Linked Data

• dbSNP Id: rs866801502
• gnomAD v4: 9-131523447-T-C
• MyVariant Identifiers: chr9:g.134398834T>C (hg19) ; chr9:g.131523447T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131523447T>C , CM000671.2:g.131523447T>C	GRCh38
NC_000009.11:g.134398834T>C , CM000671.1:g.134398834T>C	GRCh37
NC_000009.10:g.133388655T>C	NCBI36
NG_008896.1:g.25546T>C
NG_008896.2:g.25546T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341012.13:c.*341T>C	ENSP00000343034.7:n.*341T>C
ENST00000404875.7:n.3059T>C
ENST00000677295.2:c.*2863T>C	ENSP00000504346.2:n.*2863T>C
ENST00000678264.2:c.*2702T>C	ENSP00000503157.2:n.*2702T>C
ENST00000682070.1:n.2829T>C
ENST00000682639.1:c.240-16T>C
ENST00000682813.1:n.2916T>C
ENST00000683231.1:c.369T>C
ENST00000683392.1:n.5111T>C
ENST00000683900.1:n.4419T>C
ENST00000684062.1:n.3185T>C
ENST00000684399.1:c.334T>C
ENST00000684579.1:n.4365T>C
ENST00000341012.12:c.*341T>C	ENSP00000343034.7:n.*341T>C
ENST00000372220.5:c.*341T>C	ENSP00000361294.5:n.*341T>C
ENST00000372228.9:c.*341T>C	ENSP00000361302.3:n.*341T>C
ENST00000402686.8:c.*341T>C MANE Select	ENSP00000385797.4:n.*341T>C
ENST00000676640.1:c.*341T>C	ENSP00000503281.1:n.*341T>C
ENST00000676803.1:c.*341T>C	ENSP00000503093.1:n.*341T>C
ENST00000676835.1:c.*1734T>C	ENSP00000502911.1:n.*1734T>C
ENST00000677099.1:c.*2229T>C	ENSP00000504553.1:n.*2229T>C
ENST00000677295.1:c.*1741T>C	ENSP00000504346.1:n.*1741T>C
ENST00000677444.1:c.2464T>C
ENST00000677626.1:c.*341T>C	ENSP00000503552.1:n.*341T>C
ENST00000677853.1:c.*1527T>C	ENSP00000503488.1:n.*1527T>C
ENST00000678366.1:c.*2768T>C	ENSP00000504353.1:n.*2768T>C
ENST00000678546.1:c.*2464T>C	ENSP00000503062.1:n.*2464T>C
ENST00000678548.1:c.*2658T>C	ENSP00000503934.1:n.*2658T>C
ENST00000678626.1:n.2355T>C
ENST00000678739.1:c.*2685T>C	ENSP00000503806.1:n.*2685T>C
ENST00000678833.1:c.*2271T>C	ENSP00000503893.1:n.*2271T>C
ENST00000679023.1:c.*165T>C	ENSP00000503718.1:n.*165T>C
ENST00000679076.1:c.2138T>C
ENST00000679111.1:c.*1275T>C	ENSP00000504257.1:n.*1275T>C
ENST00000341012.11:c.*341T>C	ENSP00000343034.7:n.*341T>C
ENST00000372220.4:c.1382T>C	ENSP00000361294.4:n.1382T>C
ENST00000372228.7:c.*341T>C	ENSP00000361302.3:n.*341T>C
ENST00000402686.7:c.*341T>C	ENSP00000385797.3:n.*341T>C
ENST00000404875.6:c.*341T>C	ENSP00000384531.2:n.*341T>C
ENST00000423007.5:c.*341T>C	ENSP00000404119.1:n.*341T>C
ENST00000485278.5:n.3069T>C
NM_001077365.1:c.*341T>C	NP_001070833.1:n.*341T>C
NM_001077366.1:c.*341T>C	NP_001070834.1:n.*341T>C
NM_001136113.1:c.*341T>C	NP_001129585.1:n.*341T>C
NM_001136114.1:c.*341T>C	NP_001129586.1:n.*341T>C
NM_007171.3:c.*341T>C	NP_009102.3:n.*341T>C
XM_005272156.1:c.*341T>C	XP_005272213.1:n.*341T>C
XM_005272158.1:c.*341T>C	XP_005272215.1:n.*341T>C
XM_005272159.1:c.*341T>C	XP_005272216.1:n.*341T>C
XM_005272162.1:c.*341T>C	XP_005272219.1:n.*341T>C
XM_006716932.1:c.*341T>C	XP_006716995.1:n.*341T>C
XM_011518140.1:c.*341T>C	XP_011516442.1:n.*341T>C
XM_011518141.1:c.*341T>C	XP_011516443.1:n.*341T>C
XM_011518142.1:c.*341T>C	XP_011516444.1:n.*341T>C
XM_011518143.1:c.*341T>C	XP_011516445.1:n.*341T>C
XM_011518145.1:c.*341T>C	XP_011516447.1:n.*341T>C
XM_011518147.1:c.*341T>C	XP_011516449.1:n.*341T>C
XR_929703.1:n.2585T>C
NM_001353193.1:c.*341T>C	NP_001340122.1:n.*341T>C
NM_001353194.1:c.*341T>C	NP_001340123.1:n.*341T>C
NM_001353195.1:c.*341T>C	NP_001340124.1:n.*341T>C
NM_001353196.1:c.*341T>C	NP_001340125.1:n.*341T>C
NM_001353197.1:c.*341T>C	NP_001340126.1:n.*341T>C
NM_001353198.1:c.*341T>C	NP_001340127.1:n.*341T>C
NM_001353199.1:c.*341T>C	NP_001340128.1:n.*341T>C
NM_001353200.1:c.*341T>C	NP_001340129.1:n.*341T>C
NR_148391.1:n.2393T>C
NR_148392.1:n.2611T>C
NR_148393.1:n.2708T>C
NR_148394.1:n.2462T>C
NR_148395.1:n.2860T>C
NR_148396.1:n.2494T>C
NR_148397.1:n.2619T>C
NR_148398.1:n.2574T>C
NR_148399.1:n.2924T>C
NR_148400.1:n.2699T>C
XM_005272162.3:c.*341T>C	XP_005272219.1:n.*341T>C
XM_006716932.2:c.*341T>C	XP_006716995.1:n.*341T>C
XM_011518140.2:c.*341T>C	XP_011516442.1:n.*341T>C
XM_011518141.2:c.*341T>C	XP_011516443.1:n.*341T>C
XM_011518142.2:c.*341T>C	XP_011516444.1:n.*341T>C
XM_011518143.2:c.*341T>C	XP_011516445.1:n.*341T>C
XM_011518145.2:c.*341T>C	XP_011516447.1:n.*341T>C
XM_017014205.2:c.*341T>C	XP_016869694.1:n.*341T>C
XM_024447380.1:c.*341T>C	XP_024303148.1:n.*341T>C
XM_024447381.1:c.*341T>C	XP_024303149.1:n.*341T>C
XM_024447382.1:c.*341T>C	XP_024303150.1:n.*341T>C
XR_001746160.2:n.2513T>C
XR_001746162.2:n.2894T>C
XR_001746164.1:n.2611T>C
XR_001746166.2:n.2730T>C
NM_001077365.2:c.*341T>C MANE Select	NP_001070833.1:n.*341T>C
NM_001077366.2:c.*341T>C	NP_001070834.1:n.*341T>C
NM_001136113.2:c.*341T>C	NP_001129585.1:n.*341T>C
NM_001136114.2:c.*341T>C	NP_001129586.1:n.*341T>C
NM_001353193.2:c.*341T>C	NP_001340122.2:n.*341T>C
NM_001353194.2:c.*341T>C	NP_001340123.1:n.*341T>C
NM_001353195.2:c.*341T>C	NP_001340124.1:n.*341T>C
NM_001353196.2:c.*341T>C	NP_001340125.1:n.*341T>C
NM_001353197.2:c.*341T>C	NP_001340126.2:n.*341T>C
NM_001353198.2:c.*341T>C	NP_001340127.2:n.*341T>C
NM_001353199.2:c.*341T>C	NP_001340128.2:n.*341T>C
NM_001353200.2:c.*341T>C	NP_001340129.1:n.*341T>C
NM_001374689.1:c.*341T>C	NP_001361618.1:n.*341T>C
NM_001374690.1:c.*341T>C	NP_001361619.1:n.*341T>C
NM_001374691.1:c.*341T>C	NP_001361620.1:n.*341T>C
NM_001374692.1:c.*341T>C	NP_001361621.1:n.*341T>C
NM_001374693.1:c.*341T>C	NP_001361622.1:n.*341T>C
NM_001374695.1:c.*341T>C	NP_001361624.1:n.*341T>C
NM_007171.4:c.*341T>C	NP_009102.4:n.*341T>C
NR_148391.2:n.2377T>C
NR_148392.2:n.2595T>C
NR_148393.2:n.2692T>C
NR_148394.2:n.2446T>C
NR_148395.2:n.2844T>C
NR_148396.2:n.2478T>C
NR_148397.2:n.2603T>C
NR_148398.2:n.2558T>C
NR_148399.2:n.2908T>C
NR_148400.2:n.2683T>C