Canonical Allele Identifier: CA1630855386

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119096814C= , CM000673.2:g.119096814C=	GRCh38
NC_000011.9:g.118967524C= , CM000673.1:g.118967524C=	GRCh37
NC_000011.8:g.118472734C=	NCBI36
NG_008918.1:g.10262G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001382.4:c.*184G= MANE Select	NP_001373.2:n.*184G=
ENST00000354202.9:c.*184G= MANE Select	ENSP00000346142.4:n.*184G=
NM_001382.3:c.*184G=	NP_001373.2:n.*184G=
ENST00000354202.8:c.*184G=	ENSP00000346142.4:n.*184G=
ENST00000392834.7:c.*1116G=	ENSP00000376579.3:n.*1116G=
ENST00000409993.6:c.*184G=	ENSP00000386597.2:n.*184G=
ENST00000414373.5:c.*880G=	ENSP00000402019.1:n.*880G=
ENST00000445653.6:n.1635G=
ENST00000461999.1:n.1822G=
ENST00000481084.5:n.2040G=
ENST00000524658.2:n.1694G=
ENST00000530052.2:n.2700G=
ENST00000636404.1:c.482G=
ENST00000638850.1:c.934G=
ENST00000639704.1:c.*184G=	ENSP00000491336.1:n.*184G=
ENST00000640747.1:c.*1086G=	ENSP00000492730.1:n.*1086G=
ENST00000682191.1:n.1994G=
ENST00000682192.1:n.1857G=
ENST00000682232.1:c.*1028G=	ENSP00000507302.1:n.*1028G=
ENST00000682326.1:c.*381G=	ENSP00000508129.1:n.*381G=
ENST00000682404.1:n.2756G=
ENST00000682517.1:n.2981G=
ENST00000682652.1:n.2763G=
ENST00000682665.1:n.2355G=
ENST00000682691.1:n.2277G=
ENST00000682791.1:c.*184G=	ENSP00000507312.1:n.*184G=
ENST00000682811.1:c.*462G=	ENSP00000508196.1:n.*462G=
ENST00000682883.1:n.1515G=
ENST00000682946.1:c.*493G=	ENSP00000506856.1:n.*493G=
ENST00000683143.1:c.*1116G=	ENSP00000507168.1:n.*1116G=
ENST00000683373.1:n.1916G=
ENST00000683558.1:n.2160G=
ENST00000683567.1:n.1520G=
ENST00000683955.1:n.2167G=
ENST00000684142.1:c.*1252G=	ENSP00000508008.1:n.*1252G=
ENST00000684252.1:n.2052G=
ENST00000684255.1:c.*1282G=	ENSP00000507398.1:n.*1282G=
ENST00000684315.1:n.2222G=
ENST00000684345.1:c.*1555G=	ENSP00000507163.1:n.*1555G=
ENST00000684499.1:c.*1682G=	ENSP00000506800.1:n.*1682G=
ENST00000684682.1:c.*1386G=	ENSP00000507326.1:n.*1386G=
XM_005271422.2:c.*184G=	XP_005271479.1:n.*184G=
XM_005271422.3:c.*184G=	XP_005271479.1:n.*184G=
XM_011542648.1:c.*184G=	XP_011540950.1:n.*184G=
XM_011542648.2:c.*184G=	XP_011540950.1:n.*184G=
XM_017017293.2:c.*184G=	XP_016872782.1:n.*184G=
XM_017017294.2:c.*737G=	XP_016872783.1:n.*737G=
XM_017017295.1:c.*184G=	XP_016872784.1:n.*184G=
XR_001747785.2:n.1445G=
XR_947801.1:n.1570G=
XR_947801.2:n.1357G=