Canonical Allele Identifier: CA2616360850

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119097385-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097385A>G , CM000673.2:g.119097385A>G	GRCh38
NC_000011.9:g.118968095A>G , CM000673.1:g.118968095A>G	GRCh37
NC_000011.8:g.118473305A>G	NCBI36
NG_008918.1:g.9691T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1142T>C
ENST00000524658.2:n.1123T>C
ENST00000530052.2:n.2129T>C
ENST00000682191.1:n.1510+79T>C
ENST00000682192.1:n.1286T>C
ENST00000682232.1:c.*623-88T>C	ENSP00000507302.1:n.*623-88T>C
ENST00000682326.1:c.918-88T>C	ENSP00000508129.1:n.918-88T>C
ENST00000682404.1:n.2185T>C
ENST00000682517.1:n.2488T>C
ENST00000682652.1:n.2279+79T>C
ENST00000682665.1:n.1784T>C
ENST00000682691.1:n.1784T>C
ENST00000682791.1:c.918+79T>C	ENSP00000507312.1:n.918+79T>C
ENST00000682811.1:c.*56+79T>C	ENSP00000508196.1:n.*56+79T>C
ENST00000682883.1:n.1032-88T>C
ENST00000682946.1:c.*87+79T>C	ENSP00000506856.1:n.*87+79T>C
ENST00000683143.1:c.*710+79T>C	ENSP00000507168.1:n.*710+79T>C
ENST00000683373.1:n.1510+79T>C
ENST00000683558.1:n.1589T>C
ENST00000683567.1:n.1114+79T>C
ENST00000683955.1:n.1761+79T>C
ENST00000684142.1:c.*759T>C	ENSP00000508008.1:n.*759T>C
ENST00000684252.1:n.1481T>C
ENST00000684255.1:c.*789T>C	ENSP00000507398.1:n.*789T>C
ENST00000684315.1:n.1738+79T>C
ENST00000684345.1:c.*1062T>C	ENSP00000507163.1:n.*1062T>C
ENST00000684499.1:c.*1189T>C	ENSP00000506800.1:n.*1189T>C
ENST00000684682.1:c.*815T>C	ENSP00000507326.1:n.*815T>C
ENST00000354202.9:c.1005+79T>C MANE Select	ENSP00000346142.4:n.1005+79T>C
ENST00000636404.1:c.233-322T>C
ENST00000638850.1:c.528+60T>C
ENST00000639704.1:c.912+79T>C	ENSP00000491336.1:n.912+79T>C
ENST00000640102.1:c.*658+79T>C	ENSP00000492027.1:n.*658+79T>C
ENST00000640747.1:c.*680+79T>C	ENSP00000492730.1:n.*680+79T>C
ENST00000354202.8:c.1005+79T>C	ENSP00000346142.4:n.1005+79T>C
ENST00000392834.7:c.*710+79T>C	ENSP00000376579.3:n.*710+79T>C
ENST00000409993.6:c.1005+79T>C	ENSP00000386597.2:n.1005+79T>C
ENST00000414373.5:c.*475-88T>C	ENSP00000402019.1:n.*475-88T>C
ENST00000442480.1:c.737+79T>C	ENSP00000406591.1:n.737+79T>C
ENST00000461999.1:n.1251T>C
ENST00000481084.5:n.1634+79T>C
ENST00000524658.1:n.389T>C
ENST00000525456.5:n.898T>C
NM_001382.3:c.1005+79T>C	NP_001373.2:n.1005+79T>C
XM_005271422.2:c.1005+79T>C	XP_005271479.1:n.1005+79T>C
XM_011542648.1:c.684+79T>C	XP_011540950.1:n.684+79T>C
XR_947801.1:n.1165-88T>C
XM_005271422.3:c.1005+79T>C	XP_005271479.1:n.1005+79T>C
XM_011542648.2:c.684+79T>C	XP_011540950.1:n.684+79T>C
XM_017017293.2:c.684+79T>C	XP_016872782.1:n.684+79T>C
XM_017017294.2:c.*166T>C	XP_016872783.1:n.*166T>C
XM_017017295.1:c.489+79T>C	XP_016872784.1:n.489+79T>C
XR_001747785.2:n.1039+79T>C
XR_947801.2:n.952-88T>C
NM_001382.4:c.1005+79T>C MANE Select	NP_001373.2:n.1005+79T>C