Canonical Allele Identifier: CA2616360874

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119097445-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097445C>T , CM000673.2:g.119097445C>T	GRCh38
NC_000011.9:g.118968155C>T , CM000673.1:g.118968155C>T	GRCh37
NC_000011.8:g.118473365C>T	NCBI36
NG_008918.1:g.9631G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1082G>A
ENST00000524658.2:n.1063G>A
ENST00000530052.2:n.2069G>A
ENST00000682191.1:n.1510+19G>A
ENST00000682192.1:n.1226G>A
ENST00000682232.1:c.*623-148G>A	ENSP00000507302.1:n.*623-148G>A
ENST00000682326.1:c.918-148G>A	ENSP00000508129.1:n.918-148G>A
ENST00000682404.1:n.2125G>A
ENST00000682517.1:n.2428G>A
ENST00000682652.1:n.2279+19G>A
ENST00000682665.1:n.1724G>A
ENST00000682691.1:n.1724G>A
ENST00000682791.1:c.918+19G>A	ENSP00000507312.1:n.918+19G>A
ENST00000682811.1:c.*56+19G>A	ENSP00000508196.1:n.*56+19G>A
ENST00000682883.1:n.1032-148G>A
ENST00000682946.1:c.*87+19G>A	ENSP00000506856.1:n.*87+19G>A
ENST00000683143.1:c.*710+19G>A	ENSP00000507168.1:n.*710+19G>A
ENST00000683373.1:n.1510+19G>A
ENST00000683558.1:n.1529G>A
ENST00000683567.1:n.1114+19G>A
ENST00000683955.1:n.1761+19G>A
ENST00000684142.1:c.*699G>A	ENSP00000508008.1:n.*699G>A
ENST00000684252.1:n.1421G>A
ENST00000684255.1:c.*729G>A	ENSP00000507398.1:n.*729G>A
ENST00000684315.1:n.1738+19G>A
ENST00000684345.1:c.*1002G>A	ENSP00000507163.1:n.*1002G>A
ENST00000684499.1:c.*1129G>A	ENSP00000506800.1:n.*1129G>A
ENST00000684682.1:c.*755G>A	ENSP00000507326.1:n.*755G>A
ENST00000354202.9:c.1005+19G>A MANE Select	ENSP00000346142.4:n.1005+19G>A
ENST00000636404.1:c.233-382G>A
ENST00000638850.1:c.528G>A
ENST00000639704.1:c.912+19G>A	ENSP00000491336.1:n.912+19G>A
ENST00000640102.1:c.*658+19G>A	ENSP00000492027.1:n.*658+19G>A
ENST00000640747.1:c.*680+19G>A	ENSP00000492730.1:n.*680+19G>A
ENST00000354202.8:c.1005+19G>A	ENSP00000346142.4:n.1005+19G>A
ENST00000392834.7:c.*710+19G>A	ENSP00000376579.3:n.*710+19G>A
ENST00000409993.6:c.1005+19G>A	ENSP00000386597.2:n.1005+19G>A
ENST00000414373.5:c.*475-148G>A	ENSP00000402019.1:n.*475-148G>A
ENST00000442480.1:c.737+19G>A	ENSP00000406591.1:n.737+19G>A
ENST00000461999.1:n.1191G>A
ENST00000481084.5:n.1634+19G>A
ENST00000524658.1:n.329G>A
ENST00000525456.5:n.838G>A
NM_001382.3:c.1005+19G>A	NP_001373.2:n.1005+19G>A
XM_005271422.2:c.1005+19G>A	XP_005271479.1:n.1005+19G>A
XM_011542648.1:c.684+19G>A	XP_011540950.1:n.684+19G>A
XR_947801.1:n.1165-148G>A
XM_005271422.3:c.1005+19G>A	XP_005271479.1:n.1005+19G>A
XM_011542648.2:c.684+19G>A	XP_011540950.1:n.684+19G>A
XM_017017293.2:c.684+19G>A	XP_016872782.1:n.684+19G>A
XM_017017294.2:c.*106G>A	XP_016872783.1:n.*106G>A
XM_017017295.1:c.489+19G>A	XP_016872784.1:n.489+19G>A
XR_001747785.2:n.1039+19G>A
XR_947801.2:n.952-148G>A
NM_001382.4:c.1005+19G>A MANE Select	NP_001373.2:n.1005+19G>A