Canonical Allele Identifier: CA2003808804

Gene: DPAGT1

Linked Data

• dbSNP Id: rs1946418021

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097426T>G , CM000673.2:g.119097426T>G	GRCh38
NC_000011.9:g.118968136T>G , CM000673.1:g.118968136T>G	GRCh37
NC_000011.8:g.118473346T>G	NCBI36
NG_008918.1:g.9650A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1101A>C
ENST00000524658.2:n.1082A>C
ENST00000530052.2:n.2088A>C
ENST00000682191.1:n.1510+38A>C
ENST00000682192.1:n.1245A>C
ENST00000682232.1:c.*623-129A>C	ENSP00000507302.1:n.*623-129A>C
ENST00000682326.1:c.918-129A>C	ENSP00000508129.1:n.918-129A>C
ENST00000682404.1:n.2144A>C
ENST00000682517.1:n.2447A>C
ENST00000682652.1:n.2279+38A>C
ENST00000682665.1:n.1743A>C
ENST00000682691.1:n.1743A>C
ENST00000682791.1:c.918+38A>C	ENSP00000507312.1:n.918+38A>C
ENST00000682811.1:c.*56+38A>C	ENSP00000508196.1:n.*56+38A>C
ENST00000682883.1:n.1032-129A>C
ENST00000682946.1:c.*87+38A>C	ENSP00000506856.1:n.*87+38A>C
ENST00000683143.1:c.*710+38A>C	ENSP00000507168.1:n.*710+38A>C
ENST00000683373.1:n.1510+38A>C
ENST00000683558.1:n.1548A>C
ENST00000683567.1:n.1114+38A>C
ENST00000683955.1:n.1761+38A>C
ENST00000684142.1:c.*718A>C	ENSP00000508008.1:n.*718A>C
ENST00000684252.1:n.1440A>C
ENST00000684255.1:c.*748A>C	ENSP00000507398.1:n.*748A>C
ENST00000684315.1:n.1738+38A>C
ENST00000684345.1:c.*1021A>C	ENSP00000507163.1:n.*1021A>C
ENST00000684499.1:c.*1148A>C	ENSP00000506800.1:n.*1148A>C
ENST00000684682.1:c.*774A>C	ENSP00000507326.1:n.*774A>C
ENST00000354202.9:c.1005+38A>C MANE Select	ENSP00000346142.4:n.1005+38A>C
ENST00000636404.1:c.233-363A>C
ENST00000638850.1:c.528+19A>C
ENST00000639704.1:c.912+38A>C	ENSP00000491336.1:n.912+38A>C
ENST00000640102.1:c.*658+38A>C	ENSP00000492027.1:n.*658+38A>C
ENST00000640747.1:c.*680+38A>C	ENSP00000492730.1:n.*680+38A>C
ENST00000354202.8:c.1005+38A>C	ENSP00000346142.4:n.1005+38A>C
ENST00000392834.7:c.*710+38A>C	ENSP00000376579.3:n.*710+38A>C
ENST00000409993.6:c.1005+38A>C	ENSP00000386597.2:n.1005+38A>C
ENST00000414373.5:c.*475-129A>C	ENSP00000402019.1:n.*475-129A>C
ENST00000442480.1:c.737+38A>C	ENSP00000406591.1:n.737+38A>C
ENST00000461999.1:n.1210A>C
ENST00000481084.5:n.1634+38A>C
ENST00000524658.1:n.348A>C
ENST00000525456.5:n.857A>C
NM_001382.3:c.1005+38A>C	NP_001373.2:n.1005+38A>C
XM_005271422.2:c.1005+38A>C	XP_005271479.1:n.1005+38A>C
XM_011542648.1:c.684+38A>C	XP_011540950.1:n.684+38A>C
XR_947801.1:n.1165-129A>C
XM_005271422.3:c.1005+38A>C	XP_005271479.1:n.1005+38A>C
XM_011542648.2:c.684+38A>C	XP_011540950.1:n.684+38A>C
XM_017017293.2:c.684+38A>C	XP_016872782.1:n.684+38A>C
XM_017017294.2:c.*125A>C	XP_016872783.1:n.*125A>C
XM_017017295.1:c.489+38A>C	XP_016872784.1:n.489+38A>C
XR_001747785.2:n.1039+38A>C
XR_947801.2:n.952-129A>C
NM_001382.4:c.1005+38A>C MANE Select	NP_001373.2:n.1005+38A>C