Canonical Allele Identifier: CA2616355474

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119100113-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100113C>A , CM000673.2:g.119100113C>A	GRCh38
NC_000011.9:g.118970823C>A , CM000673.1:g.118970823C>A	GRCh37
NC_000011.8:g.118476033C>A	NCBI36
NG_008918.1:g.6963G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.819+149G>T
ENST00000530052.2:n.1385+149G>T
ENST00000682191.1:n.845+149G>T
ENST00000682192.1:n.845+149G>T
ENST00000682232.1:c.*348+149G>T	ENSP00000507302.1:n.*348+149G>T
ENST00000682326.1:c.643+149G>T	ENSP00000508129.1:n.643+149G>T
ENST00000682404.1:n.1385+149G>T
ENST00000682517.1:n.1385+149G>T
ENST00000682652.1:n.1614+149G>T
ENST00000682665.1:n.1040+149G>T
ENST00000682691.1:n.1040+149G>T
ENST00000682791.1:c.556+149G>T	ENSP00000507312.1:n.556+149G>T
ENST00000682811.1:c.643+149G>T	ENSP00000508196.1:n.643+149G>T
ENST00000682883.1:n.946+149G>T
ENST00000682946.1:c.643+149G>T	ENSP00000506856.1:n.643+149G>T
ENST00000683143.1:c.*348+149G>T	ENSP00000507168.1:n.*348+149G>T
ENST00000683373.1:n.845+149G>T
ENST00000683558.1:n.845+149G>T
ENST00000683567.1:n.870+149G>T
ENST00000683955.1:n.1040+149G>T
ENST00000684142.1:c.*318+149G>T	ENSP00000508008.1:n.*318+149G>T
ENST00000684252.1:n.1040+149G>T
ENST00000684255.1:c.*348+149G>T	ENSP00000507398.1:n.*348+149G>T
ENST00000684315.1:n.1376+149G>T
ENST00000684345.1:c.*318+149G>T	ENSP00000507163.1:n.*318+149G>T
ENST00000684499.1:c.*748+149G>T	ENSP00000506800.1:n.*748+149G>T
ENST00000684682.1:c.*71+149G>T	ENSP00000507326.1:n.*71+149G>T
ENST00000354202.9:c.643+149G>T MANE Select	ENSP00000346142.4:n.643+149G>T
ENST00000636404.1:c.147+149G>T
ENST00000638850.1:c.147+149G>T
ENST00000639704.1:c.550+149G>T	ENSP00000491336.1:n.550+149G>T
ENST00000640102.1:c.*296+149G>T	ENSP00000492027.1:n.*296+149G>T
ENST00000640747.1:c.*318+149G>T	ENSP00000492730.1:n.*318+149G>T
ENST00000354202.8:c.643+149G>T	ENSP00000346142.4:n.643+149G>T
ENST00000392834.7:c.*348+149G>T	ENSP00000376579.3:n.*348+149G>T
ENST00000409993.6:c.643+149G>T	ENSP00000386597.2:n.643+149G>T
ENST00000414373.5:c.*389+149G>T	ENSP00000402019.1:n.*389+149G>T
ENST00000442480.1:c.493+149G>T	ENSP00000406591.1:n.493+149G>T
ENST00000461999.1:n.148+149G>T
ENST00000481084.5:n.1272+149G>T
ENST00000525456.5:n.646+149G>T
ENST00000530052.1:n.541+149G>T
ENST00000533687.1:n.655+149G>T
NM_001382.3:c.643+149G>T	NP_001373.2:n.643+149G>T
XM_005271422.2:c.643+149G>T	XP_005271479.1:n.643+149G>T
XM_011542648.1:c.322+149G>T	XP_011540950.1:n.322+149G>T
XR_947801.1:n.1079+149G>T
XM_005271422.3:c.643+149G>T	XP_005271479.1:n.643+149G>T
XM_011542648.2:c.322+149G>T	XP_011540950.1:n.322+149G>T
XM_017017293.2:c.322+149G>T	XP_016872782.1:n.322+149G>T
XM_017017294.2:c.643+149G>T	XP_016872783.1:n.643+149G>T
XM_017017295.1:c.127+149G>T	XP_016872784.1:n.127+149G>T
XR_001747785.2:n.866+149G>T
XR_947801.2:n.866+149G>T
NM_001382.4:c.643+149G>T MANE Select	NP_001373.2:n.643+149G>T