Canonical Allele Identifier: CA2003808817

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097465T= , CM000673.2:g.119097465T=	GRCh38
NC_000011.9:g.118968175T= , CM000673.1:g.118968175T=	GRCh37
NC_000011.8:g.118473385T=	NCBI36
NG_008918.1:g.9611A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1062A=
ENST00000524658.2:n.1043A=
ENST00000530052.2:n.2049A=
ENST00000682191.1:n.1509A=
ENST00000682192.1:n.1206A=
ENST00000682232.1:c.*623-168A=	ENSP00000507302.1:n.*623-168A=
ENST00000682326.1:c.918-168A=	ENSP00000508129.1:n.918-168A=
ENST00000682404.1:n.2105A=
ENST00000682517.1:n.2408A=
ENST00000682652.1:n.2278A=
ENST00000682665.1:n.1704A=
ENST00000682691.1:n.1704A=
ENST00000682791.1:c.917A=	ENSP00000507312.1:p.Lys306=
ENST00000682811.1:c.*55A=	ENSP00000508196.1:n.*55A=
ENST00000682883.1:n.1032-168A=
ENST00000682946.1:c.*86A=	ENSP00000506856.1:n.*86A=
ENST00000683143.1:c.*709A=	ENSP00000507168.1:n.*709A=
ENST00000683373.1:n.1509A=
ENST00000683558.1:n.1509A=
ENST00000683567.1:n.1113A=
ENST00000683955.1:n.1760A=
ENST00000684142.1:c.*679A=	ENSP00000508008.1:n.*679A=
ENST00000684252.1:n.1401A=
ENST00000684255.1:c.*709A=	ENSP00000507398.1:n.*709A=
ENST00000684315.1:n.1737A=
ENST00000684345.1:c.*982A=	ENSP00000507163.1:n.*982A=
ENST00000684499.1:c.*1109A=	ENSP00000506800.1:n.*1109A=
ENST00000684682.1:c.*735A=	ENSP00000507326.1:n.*735A=
ENST00000354202.9:c.1004A= MANE Select	ENSP00000346142.4:p.Lys335=
ENST00000636404.1:c.233-402A=
ENST00000638850.1:c.508A=
ENST00000639704.1:c.911A=	ENSP00000491336.1:p.Lys304=
ENST00000640102.1:c.*657A=	ENSP00000492027.1:n.*657A=
ENST00000640747.1:c.*679A=	ENSP00000492730.1:n.*679A=
ENST00000354202.8:c.1004A=	ENSP00000346142.4:p.Lys335=
ENST00000392834.7:c.*709A=	ENSP00000376579.3:n.*709A=
ENST00000409993.6:c.1004A=	ENSP00000386597.2:p.Lys335=
ENST00000414373.5:c.*475-168A=	ENSP00000402019.1:n.*475-168A=
ENST00000442480.1:c.736A=	ENSP00000406591.1:n.736A=
ENST00000461999.1:n.1171A=
ENST00000481084.5:n.1633A=
ENST00000524658.1:n.309A=
ENST00000525456.5:n.818A=
NM_001382.3:c.1004A=	NP_001373.2:p.Lys335=
XM_005271422.2:c.1004A=	XP_005271479.1:p.Lys335=
XM_011542648.1:c.683A=	XP_011540950.1:p.Lys228=
XR_947801.1:n.1165-168A=
XM_005271422.3:c.1004A=	XP_005271479.1:p.Lys335=
XM_011542648.2:c.683A=	XP_011540950.1:p.Lys228=
XM_017017293.2:c.683A=	XP_016872782.1:p.Lys228=
XM_017017294.2:c.*86A=	XP_016872783.1:n.*86A=
XM_017017295.1:c.488A=	XP_016872784.1:p.Lys163=
XR_001747785.2:n.1038A=
XR_947801.2:n.952-168A=
NM_001382.4:c.1004A= MANE Select	NP_001373.2:p.Lys335=