Canonical Allele Identifier: CA2616360861

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119097398-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097398C>A , CM000673.2:g.119097398C>A	GRCh38
NC_000011.9:g.118968108C>A , CM000673.1:g.118968108C>A	GRCh37
NC_000011.8:g.118473318C>A	NCBI36
NG_008918.1:g.9678G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1129G>T
ENST00000524658.2:n.1110G>T
ENST00000530052.2:n.2116G>T
ENST00000682191.1:n.1510+66G>T
ENST00000682192.1:n.1273G>T
ENST00000682232.1:c.*623-101G>T	ENSP00000507302.1:n.*623-101G>T
ENST00000682326.1:c.918-101G>T	ENSP00000508129.1:n.918-101G>T
ENST00000682404.1:n.2172G>T
ENST00000682517.1:n.2475G>T
ENST00000682652.1:n.2279+66G>T
ENST00000682665.1:n.1771G>T
ENST00000682691.1:n.1771G>T
ENST00000682791.1:c.918+66G>T	ENSP00000507312.1:n.918+66G>T
ENST00000682811.1:c.*56+66G>T	ENSP00000508196.1:n.*56+66G>T
ENST00000682883.1:n.1032-101G>T
ENST00000682946.1:c.*87+66G>T	ENSP00000506856.1:n.*87+66G>T
ENST00000683143.1:c.*710+66G>T	ENSP00000507168.1:n.*710+66G>T
ENST00000683373.1:n.1510+66G>T
ENST00000683558.1:n.1576G>T
ENST00000683567.1:n.1114+66G>T
ENST00000683955.1:n.1761+66G>T
ENST00000684142.1:c.*746G>T	ENSP00000508008.1:n.*746G>T
ENST00000684252.1:n.1468G>T
ENST00000684255.1:c.*776G>T	ENSP00000507398.1:n.*776G>T
ENST00000684315.1:n.1738+66G>T
ENST00000684345.1:c.*1049G>T	ENSP00000507163.1:n.*1049G>T
ENST00000684499.1:c.*1176G>T	ENSP00000506800.1:n.*1176G>T
ENST00000684682.1:c.*802G>T	ENSP00000507326.1:n.*802G>T
ENST00000354202.9:c.1005+66G>T MANE Select	ENSP00000346142.4:n.1005+66G>T
ENST00000636404.1:c.233-335G>T
ENST00000638850.1:c.528+47G>T
ENST00000639704.1:c.912+66G>T	ENSP00000491336.1:n.912+66G>T
ENST00000640102.1:c.*658+66G>T	ENSP00000492027.1:n.*658+66G>T
ENST00000640747.1:c.*680+66G>T	ENSP00000492730.1:n.*680+66G>T
ENST00000354202.8:c.1005+66G>T	ENSP00000346142.4:n.1005+66G>T
ENST00000392834.7:c.*710+66G>T	ENSP00000376579.3:n.*710+66G>T
ENST00000409993.6:c.1005+66G>T	ENSP00000386597.2:n.1005+66G>T
ENST00000414373.5:c.*475-101G>T	ENSP00000402019.1:n.*475-101G>T
ENST00000442480.1:c.737+66G>T	ENSP00000406591.1:n.737+66G>T
ENST00000461999.1:n.1238G>T
ENST00000481084.5:n.1634+66G>T
ENST00000524658.1:n.376G>T
ENST00000525456.5:n.885G>T
NM_001382.3:c.1005+66G>T	NP_001373.2:n.1005+66G>T
XM_005271422.2:c.1005+66G>T	XP_005271479.1:n.1005+66G>T
XM_011542648.1:c.684+66G>T	XP_011540950.1:n.684+66G>T
XR_947801.1:n.1165-101G>T
XM_005271422.3:c.1005+66G>T	XP_005271479.1:n.1005+66G>T
XM_011542648.2:c.684+66G>T	XP_011540950.1:n.684+66G>T
XM_017017293.2:c.684+66G>T	XP_016872782.1:n.684+66G>T
XM_017017294.2:c.*153G>T	XP_016872783.1:n.*153G>T
XM_017017295.1:c.489+66G>T	XP_016872784.1:n.489+66G>T
XR_001747785.2:n.1039+66G>T
XR_947801.2:n.952-101G>T
NM_001382.4:c.1005+66G>T MANE Select	NP_001373.2:n.1005+66G>T