Canonical Allele Identifier: CA382914241

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971025T>A (hg19) ; chr11:g.119100315T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100315T>A , CM000673.2:g.119100315T>A	GRCh38
NC_000011.9:g.118971025T>A , CM000673.1:g.118971025T>A	GRCh37
NC_000011.8:g.118476235T>A	NCBI36
NG_008918.1:g.6761A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.766A>T
ENST00000530052.2:n.1332A>T
ENST00000682191.1:n.792A>T
ENST00000682192.1:n.792A>T
ENST00000682232.1:c.*295A>T	ENSP00000507302.1:n.*295A>T
ENST00000682326.1:c.590A>T	ENSP00000508129.1:p.Gln197Leu
ENST00000682404.1:n.1332A>T
ENST00000682517.1:n.1332A>T
ENST00000682652.1:n.1561A>T
ENST00000682665.1:n.987A>T
ENST00000682691.1:n.987A>T
ENST00000682791.1:c.503A>T	ENSP00000507312.1:p.Gln168Leu
ENST00000682811.1:c.590A>T	ENSP00000508196.1:p.Gln197Leu
ENST00000682883.1:n.893A>T
ENST00000682946.1:c.590A>T	ENSP00000506856.1:p.Gln197Leu
ENST00000683143.1:c.*295A>T	ENSP00000507168.1:n.*295A>T
ENST00000683373.1:n.792A>T
ENST00000683558.1:n.792A>T
ENST00000683567.1:n.817A>T
ENST00000683955.1:n.987A>T
ENST00000684142.1:c.*265A>T	ENSP00000508008.1:n.*265A>T
ENST00000684252.1:n.987A>T
ENST00000684255.1:c.*295A>T	ENSP00000507398.1:n.*295A>T
ENST00000684315.1:n.1323A>T
ENST00000684345.1:c.*265A>T	ENSP00000507163.1:n.*265A>T
ENST00000684499.1:c.*695A>T	ENSP00000506800.1:n.*695A>T
ENST00000684682.1:c.*18A>T	ENSP00000507326.1:n.*18A>T
ENST00000354202.9:c.590A>T MANE Select	ENSP00000346142.4:p.Gln197Leu
ENST00000636404.1:c.94A>T
ENST00000638850.1:c.94A>T
ENST00000639704.1:c.497A>T	ENSP00000491336.1:p.Gln166Leu
ENST00000640102.1:c.*243A>T	ENSP00000492027.1:n.*243A>T
ENST00000640747.1:c.*265A>T	ENSP00000492730.1:n.*265A>T
ENST00000354202.8:c.590A>T	ENSP00000346142.4:p.Gln197Leu
ENST00000392834.7:c.*295A>T	ENSP00000376579.3:n.*295A>T
ENST00000409993.6:c.590A>T	ENSP00000386597.2:p.Gln197Leu
ENST00000414373.5:c.*336A>T	ENSP00000402019.1:n.*336A>T
ENST00000442480.1:c.440A>T	ENSP00000406591.1:p.Gln147Leu
ENST00000461999.1:n.95A>T
ENST00000481084.5:n.1219A>T
ENST00000525456.5:n.593A>T
ENST00000530052.1:n.488A>T
ENST00000533687.1:n.602A>T
NM_001382.3:c.590A>T	NP_001373.2:p.Gln197Leu
XM_005271422.2:c.590A>T	XP_005271479.1:p.Gln197Leu
XM_011542648.1:c.269A>T	XP_011540950.1:p.Gln90Leu
XR_947801.1:n.1026A>T
XM_005271422.3:c.590A>T	XP_005271479.1:p.Gln197Leu
XM_011542648.2:c.269A>T	XP_011540950.1:p.Gln90Leu
XM_017017293.2:c.269A>T	XP_016872782.1:p.Gln90Leu
XM_017017294.2:c.590A>T	XP_016872783.1:p.Gln197Leu
XM_017017295.1:c.74A>T	XP_016872784.1:p.Gln25Leu
XR_001747785.2:n.813A>T
XR_947801.2:n.813A>T
NM_001382.4:c.590A>T MANE Select	NP_001373.2:p.Gln197Leu