Canonical Allele Identifier: CA467424014

Gene: POMT1

Linked Data

• MyVariant Identifiers: chr9:g.134397454C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131522067C>T , CM000671.2:g.131522067C>T	GRCh38
NC_000009.11:g.134397454C>T , CM000671.1:g.134397454C>T	GRCh37
NC_000009.10:g.133387275C>T	NCBI36
NG_008896.1:g.24166C>T
NG_008896.2:g.24166C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000341012.13:c.1684C>T	ENSP00000343034.7:p.Leu562=
ENST00000404875.7:n.2386C>T
ENST00000423007.6:c.1903C>T	ENSP00000404119.2:p.Leu635=
ENST00000677295.2:c.*2190C>T	ENSP00000504346.2:n.*2190C>T
ENST00000678264.2:c.*2029C>T	ENSP00000503157.2:n.*2029C>T
ENST00000682070.1:n.2291-135C>T
ENST00000682813.1:n.2250C>T
ENST00000683392.1:n.4573-135C>T
ENST00000683712.1:n.2251C>T
ENST00000683900.1:n.3746C>T
ENST00000684062.1:n.2512C>T
ENST00000684579.1:n.3692C>T
ENST00000684679.1:n.1073C>T
ENST00000341012.12:c.1684C>T	ENSP00000343034.7:p.Leu562=
ENST00000372220.5:c.715C>T	ENSP00000361294.5:p.Leu239=
ENST00000372228.9:c.1912C>T	ENSP00000361302.3:p.Leu638=
ENST00000402686.8:c.1846C>T MANE Select	ENSP00000385797.4:p.Leu616=
ENST00000676640.1:c.1846C>T	ENSP00000503281.1:p.Leu616=
ENST00000676803.1:c.907C>T	ENSP00000503093.1:p.Leu303=
ENST00000676835.1:c.*1061C>T	ENSP00000502911.1:n.*1061C>T
ENST00000677029.1:c.1390C>T	ENSP00000502936.1:p.Leu464=
ENST00000677099.1:c.*1556C>T	ENSP00000504553.1:n.*1556C>T
ENST00000677216.1:c.1495C>T	ENSP00000503772.1:p.Leu499=
ENST00000677221.1:n.871C>T
ENST00000677295.1:c.*1203-135C>T	ENSP00000504346.1:n.*1203-135C>T
ENST00000677444.1:c.1791C>T
ENST00000677586.1:n.1213C>T
ENST00000677626.1:c.1495C>T	ENSP00000503552.1:p.Leu499=
ENST00000677853.1:c.*854C>T	ENSP00000503488.1:n.*854C>T
ENST00000678202.1:n.1005C>T
ENST00000678264.1:c.*1223C>T	ENSP00000503157.1:n.*1223C>T
ENST00000678303.1:c.1756C>T	ENSP00000503696.1:p.Leu586=
ENST00000678366.1:c.*2095C>T	ENSP00000504353.1:n.*2095C>T
ENST00000678546.1:c.*1791C>T	ENSP00000503062.1:n.*1791C>T
ENST00000678548.1:c.*1985C>T	ENSP00000503934.1:n.*1985C>T
ENST00000678626.1:n.1682C>T
ENST00000678739.1:c.*2147-135C>T	ENSP00000503806.1:n.*2147-135C>T
ENST00000678833.1:c.*1598C>T	ENSP00000503893.1:n.*1598C>T
ENST00000679023.1:c.1684C>T	ENSP00000503718.1:p.Leu562=
ENST00000679076.1:c.1465C>T
ENST00000679111.1:c.*602C>T	ENSP00000504257.1:n.*602C>T
ENST00000679189.1:c.1495C>T	ENSP00000503356.1:p.Leu499=
ENST00000341012.11:c.1684C>T	ENSP00000343034.7:p.Leu562=
ENST00000372220.4:c.709C>T	ENSP00000361294.4:p.Leu237=
ENST00000372228.7:c.1912C>T	ENSP00000361302.3:p.Leu638=
ENST00000402686.7:c.1846C>T	ENSP00000385797.3:p.Leu616=
ENST00000404875.6:c.1495C>T	ENSP00000384531.2:p.Leu499=
ENST00000423007.5:c.1846C>T	ENSP00000404119.1:p.Leu616=
ENST00000485278.5:n.2396C>T
ENST00000494883.1:n.389C>T
NM_001077365.1:c.1846C>T	NP_001070833.1:p.Leu616=
NM_001077366.1:c.1684C>T	NP_001070834.1:p.Leu562=
NM_001136113.1:c.1846C>T	NP_001129585.1:p.Leu616=
NM_001136114.1:c.1495C>T	NP_001129586.1:p.Leu499=
NM_007171.3:c.1912C>T	NP_009102.3:p.Leu638=
XM_005272156.1:c.1912C>T	XP_005272213.1:p.Leu638=
XM_005272158.1:c.1750C>T	XP_005272215.1:p.Leu584=
XM_005272159.1:c.1561C>T	XP_005272216.1:p.Leu521=
XM_005272162.1:c.715C>T	XP_005272219.1:p.Leu239=
XM_006716932.1:c.1561C>T	XP_006716995.1:p.Leu521=
XM_011518140.1:c.1765C>T	XP_011516442.1:p.Leu589=
XM_011518141.1:c.1699C>T	XP_011516443.1:p.Leu567=
XM_011518142.1:c.1603C>T	XP_011516444.1:p.Leu535=
XM_011518143.1:c.1597C>T	XP_011516445.1:p.Leu533=
XM_011518145.1:c.1456C>T	XP_011516447.1:p.Leu486=
XM_011518147.1:c.784C>T	XP_011516449.1:p.Leu262=
XR_929703.1:n.2088C>T
NM_001353193.1:c.1912C>T	NP_001340122.1:p.Leu638=
NM_001353194.1:c.1684C>T	NP_001340123.1:p.Leu562=
NM_001353195.1:c.1495C>T	NP_001340124.1:p.Leu499=
NM_001353196.1:c.1756C>T	NP_001340125.1:p.Leu586=
NM_001353197.1:c.1750C>T	NP_001340126.1:p.Leu584=
NM_001353198.1:c.1750C>T	NP_001340127.1:p.Leu584=
NM_001353199.1:c.1561C>T	NP_001340128.1:p.Leu521=
NM_001353200.1:c.1390C>T	NP_001340129.1:p.Leu464=
NR_148391.1:n.1896C>T
NR_148392.1:n.2114C>T
NR_148393.1:n.2035C>T
NR_148394.1:n.1789C>T
NR_148395.1:n.2187C>T
NR_148396.1:n.1821C>T
NR_148397.1:n.1946C>T
NR_148398.1:n.1901C>T
NR_148399.1:n.2427C>T
NR_148400.1:n.2026C>T
XM_005272162.3:c.715C>T	XP_005272219.1:p.Leu239=
XM_006716932.2:c.1561C>T	XP_006716995.1:p.Leu521=
XM_011518140.2:c.1765C>T	XP_011516442.1:p.Leu589=
XM_011518141.2:c.1699C>T	XP_011516443.1:p.Leu567=
XM_011518142.2:c.1603C>T	XP_011516444.1:p.Leu535=
XM_011518143.2:c.1597C>T	XP_011516445.1:p.Leu533=
XM_011518145.2:c.1456C>T	XP_011516447.1:p.Leu486=
XM_017014205.2:c.715C>T	XP_016869694.1:p.Leu239=
XM_024447380.1:c.715C>T	XP_024303148.1:p.Leu239=
XM_024447381.1:c.1021C>T	XP_024303149.1:p.Leu341=
XM_024447382.1:c.715C>T	XP_024303150.1:p.Leu239=
XR_001746160.2:n.2016C>T
XR_001746162.2:n.2221C>T
XR_001746164.1:n.1938C>T
XR_001746166.2:n.2233C>T
NM_001077365.2:c.1846C>T MANE Select	NP_001070833.1:p.Leu616=
NM_001077366.2:c.1684C>T	NP_001070834.1:p.Leu562=
NM_001136113.2:c.1846C>T	NP_001129585.1:p.Leu616=
NM_001136114.2:c.1495C>T	NP_001129586.1:p.Leu499=
NM_001353193.2:c.1912C>T	NP_001340122.2:p.Leu638=
NM_001353194.2:c.1684C>T	NP_001340123.1:p.Leu562=
NM_001353195.2:c.1495C>T	NP_001340124.1:p.Leu499=
NM_001353196.2:c.1756C>T	NP_001340125.1:p.Leu586=
NM_001353197.2:c.1750C>T	NP_001340126.2:p.Leu584=
NM_001353198.2:c.1750C>T	NP_001340127.2:p.Leu584=
NM_001353199.2:c.1561C>T	NP_001340128.2:p.Leu521=
NM_001353200.2:c.1390C>T	NP_001340129.1:p.Leu464=
NM_001374689.1:c.1834C>T	NP_001361618.1:p.Leu612=
NM_001374690.1:c.1627C>T	NP_001361619.1:p.Leu543=
NM_001374691.1:c.1495C>T	NP_001361620.1:p.Leu499=
NM_001374692.1:c.1495C>T	NP_001361621.1:p.Leu499=
NM_001374693.1:c.1495C>T	NP_001361622.1:p.Leu499=
NM_001374695.1:c.1456C>T	NP_001361624.1:p.Leu486=
NM_007171.4:c.1912C>T	NP_009102.4:p.Leu638=
NR_148391.2:n.1880C>T
NR_148392.2:n.2098C>T
NR_148393.2:n.2019C>T
NR_148394.2:n.1773C>T
NR_148395.2:n.2171C>T
NR_148396.2:n.1805C>T
NR_148397.2:n.1930C>T
NR_148398.2:n.1885C>T
NR_148399.2:n.2411C>T
NR_148400.2:n.2010C>T