Canonical Allele Identifier: CA2616361122

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119097610-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097610G>T , CM000673.2:g.119097610G>T	GRCh38
NC_000011.9:g.118968320G>T , CM000673.1:g.118968320G>T	GRCh37
NC_000011.8:g.118473530G>T	NCBI36
NG_008918.1:g.9466C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-59C>A
ENST00000524658.2:n.957-59C>A
ENST00000530052.2:n.1904C>A
ENST00000682191.1:n.1364C>A
ENST00000682192.1:n.1120-59C>A
ENST00000682232.1:c.*622+245C>A	ENSP00000507302.1:n.*622+245C>A
ENST00000682326.1:c.917+245C>A	ENSP00000508129.1:n.917+245C>A
ENST00000682404.1:n.2019-59C>A
ENST00000682517.1:n.2263C>A
ENST00000682652.1:n.2133C>A
ENST00000682665.1:n.1559C>A
ENST00000682691.1:n.1559C>A
ENST00000682791.1:c.831-59C>A	ENSP00000507312.1:n.831-59C>A
ENST00000682811.1:c.800-59C>A	ENSP00000508196.1:n.800-59C>A
ENST00000682883.1:n.1032-313C>A
ENST00000682946.1:c.729-59C>A	ENSP00000506856.1:n.729-59C>A
ENST00000683143.1:c.*623-59C>A	ENSP00000507168.1:n.*623-59C>A
ENST00000683373.1:n.1364C>A
ENST00000683558.1:n.1364C>A
ENST00000683567.1:n.1027-59C>A
ENST00000683955.1:n.1674-59C>A
ENST00000684142.1:c.*593-59C>A	ENSP00000508008.1:n.*593-59C>A
ENST00000684252.1:n.1315-59C>A
ENST00000684255.1:c.*623-59C>A	ENSP00000507398.1:n.*623-59C>A
ENST00000684315.1:n.1651-59C>A
ENST00000684345.1:c.*837C>A	ENSP00000507163.1:n.*837C>A
ENST00000684499.1:c.*1023-59C>A	ENSP00000506800.1:n.*1023-59C>A
ENST00000684682.1:c.*590C>A	ENSP00000507326.1:n.*590C>A
ENST00000354202.9:c.918-59C>A MANE Select	ENSP00000346142.4:n.918-59C>A
ENST00000636404.1:c.233-547C>A
ENST00000638850.1:c.422-59C>A
ENST00000639704.1:c.825-59C>A	ENSP00000491336.1:n.825-59C>A
ENST00000640102.1:c.*571-59C>A	ENSP00000492027.1:n.*571-59C>A
ENST00000640747.1:c.*593-59C>A	ENSP00000492730.1:n.*593-59C>A
ENST00000354202.8:c.918-59C>A	ENSP00000346142.4:n.918-59C>A
ENST00000392834.7:c.*623-59C>A	ENSP00000376579.3:n.*623-59C>A
ENST00000409993.6:c.918-59C>A	ENSP00000386597.2:n.918-59C>A
ENST00000414373.5:c.*475-313C>A	ENSP00000402019.1:n.*475-313C>A
ENST00000442480.1:c.650-59C>A	ENSP00000406591.1:n.650-59C>A
ENST00000461999.1:n.1026C>A
ENST00000481084.5:n.1547-59C>A
ENST00000524658.1:n.223-59C>A
ENST00000525456.5:n.732-59C>A
NM_001382.3:c.918-59C>A	NP_001373.2:n.918-59C>A
XM_005271422.2:c.918-59C>A	XP_005271479.1:n.918-59C>A
XM_011542648.1:c.597-59C>A	XP_011540950.1:n.597-59C>A
XR_947801.1:n.1165-313C>A
XM_005271422.3:c.918-59C>A	XP_005271479.1:n.918-59C>A
XM_011542648.2:c.597-59C>A	XP_011540950.1:n.597-59C>A
XM_017017293.2:c.597-59C>A	XP_016872782.1:n.597-59C>A
XM_017017294.2:c.729-59C>A	XP_016872783.1:n.729-59C>A
XM_017017295.1:c.402-59C>A	XP_016872784.1:n.402-59C>A
XR_001747785.2:n.952-59C>A
XR_947801.2:n.952-313C>A
NM_001382.4:c.918-59C>A MANE Select	NP_001373.2:n.918-59C>A