Canonical Allele Identifier: CA2003808819

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097473A= , CM000673.2:g.119097473A=	GRCh38
NC_000011.9:g.118968183A= , CM000673.1:g.118968183A=	GRCh37
NC_000011.8:g.118473393A=	NCBI36
NG_008918.1:g.9603T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1054T=
ENST00000524658.2:n.1035T=
ENST00000530052.2:n.2041T=
ENST00000682191.1:n.1501T=
ENST00000682192.1:n.1198T=
ENST00000682232.1:c.*623-176T=	ENSP00000507302.1:n.*623-176T=
ENST00000682326.1:c.918-176T=	ENSP00000508129.1:n.918-176T=
ENST00000682404.1:n.2097T=
ENST00000682517.1:n.2400T=
ENST00000682652.1:n.2270T=
ENST00000682665.1:n.1696T=
ENST00000682691.1:n.1696T=
ENST00000682791.1:c.909T=	ENSP00000507312.1:p.Phe303=
ENST00000682811.1:c.*47T=	ENSP00000508196.1:n.*47T=
ENST00000682883.1:n.1032-176T=
ENST00000682946.1:c.*78T=	ENSP00000506856.1:n.*78T=
ENST00000683143.1:c.*701T=	ENSP00000507168.1:n.*701T=
ENST00000683373.1:n.1501T=
ENST00000683558.1:n.1501T=
ENST00000683567.1:n.1105T=
ENST00000683955.1:n.1752T=
ENST00000684142.1:c.*671T=	ENSP00000508008.1:n.*671T=
ENST00000684252.1:n.1393T=
ENST00000684255.1:c.*701T=	ENSP00000507398.1:n.*701T=
ENST00000684315.1:n.1729T=
ENST00000684345.1:c.*974T=	ENSP00000507163.1:n.*974T=
ENST00000684499.1:c.*1101T=	ENSP00000506800.1:n.*1101T=
ENST00000684682.1:c.*727T=	ENSP00000507326.1:n.*727T=
ENST00000354202.9:c.996T= MANE Select	ENSP00000346142.4:p.Phe332=
ENST00000636404.1:c.233-410T=
ENST00000638850.1:c.500T=
ENST00000639704.1:c.903T=	ENSP00000491336.1:p.Phe301=
ENST00000640102.1:c.*649T=	ENSP00000492027.1:n.*649T=
ENST00000640747.1:c.*671T=	ENSP00000492730.1:n.*671T=
ENST00000354202.8:c.996T=	ENSP00000346142.4:p.Phe332=
ENST00000392834.7:c.*701T=	ENSP00000376579.3:n.*701T=
ENST00000409993.6:c.996T=	ENSP00000386597.2:p.Phe332=
ENST00000414373.5:c.*475-176T=	ENSP00000402019.1:n.*475-176T=
ENST00000442480.1:c.728T=	ENSP00000406591.1:n.728T=
ENST00000461999.1:n.1163T=
ENST00000481084.5:n.1625T=
ENST00000524658.1:n.301T=
ENST00000525456.5:n.810T=
NM_001382.3:c.996T=	NP_001373.2:p.Phe332=
XM_005271422.2:c.996T=	XP_005271479.1:p.Phe332=
XM_011542648.1:c.675T=	XP_011540950.1:p.Phe225=
XR_947801.1:n.1165-176T=
XM_005271422.3:c.996T=	XP_005271479.1:p.Phe332=
XM_011542648.2:c.675T=	XP_011540950.1:p.Phe225=
XM_017017293.2:c.675T=	XP_016872782.1:p.Phe225=
XM_017017294.2:c.*78T=	XP_016872783.1:n.*78T=
XM_017017295.1:c.480T=	XP_016872784.1:p.Phe160=
XR_001747785.2:n.1030T=
XR_947801.2:n.952-176T=
NM_001382.4:c.996T= MANE Select	NP_001373.2:p.Phe332=