Canonical Allele Identifier: CA2003810084

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100434A= , CM000673.2:g.119100434A=	GRCh38
NC_000011.9:g.118971144A= , CM000673.1:g.118971144A=	GRCh37
NC_000011.8:g.118476354A=	NCBI36
NG_008918.1:g.6642T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.673-26T=
ENST00000530052.2:n.1239-26T=
ENST00000682191.1:n.699-26T=
ENST00000682192.1:n.699-26T=
ENST00000682232.1:c.*202-26T=	ENSP00000507302.1:n.*202-26T=
ENST00000682326.1:c.497-26T=	ENSP00000508129.1:n.497-26T=
ENST00000682404.1:n.1239-26T=
ENST00000682517.1:n.1239-26T=
ENST00000682652.1:n.1468-26T=
ENST00000682665.1:n.894-26T=
ENST00000682691.1:n.894-26T=
ENST00000682791.1:c.410-26T=	ENSP00000507312.1:n.410-26T=
ENST00000682811.1:c.497-26T=	ENSP00000508196.1:n.497-26T=
ENST00000682883.1:n.800-26T=
ENST00000682946.1:c.497-26T=	ENSP00000506856.1:n.497-26T=
ENST00000683143.1:c.*202-26T=	ENSP00000507168.1:n.*202-26T=
ENST00000683373.1:n.699-26T=
ENST00000683558.1:n.699-26T=
ENST00000683567.1:n.724-26T=
ENST00000683955.1:n.894-26T=
ENST00000684142.1:c.*172-26T=	ENSP00000508008.1:n.*172-26T=
ENST00000684252.1:n.894-26T=
ENST00000684255.1:c.*202-26T=	ENSP00000507398.1:n.*202-26T=
ENST00000684315.1:n.1230-26T=
ENST00000684345.1:c.*172-26T=	ENSP00000507163.1:n.*172-26T=
ENST00000684499.1:c.*602-26T=	ENSP00000506800.1:n.*602-26T=
ENST00000684682.1:c.162-26T=	ENSP00000507326.1:n.162-26T=
ENST00000354202.9:c.497-26T= MANE Select	ENSP00000346142.4:n.497-26T=
ENST00000639704.1:c.404-26T=	ENSP00000491336.1:n.404-26T=
ENST00000640102.1:c.*150-26T=	ENSP00000492027.1:n.*150-26T=
ENST00000640747.1:c.*172-26T=	ENSP00000492730.1:n.*172-26T=
ENST00000354202.8:c.497-26T=	ENSP00000346142.4:n.497-26T=
ENST00000392834.7:c.*202-26T=	ENSP00000376579.3:n.*202-26T=
ENST00000409993.6:c.497-26T=	ENSP00000386597.2:n.497-26T=
ENST00000414373.5:c.*243-26T=	ENSP00000402019.1:n.*243-26T=
ENST00000442480.1:c.347-26T=	ENSP00000406591.1:n.347-26T=
ENST00000481084.5:n.1126-26T=
ENST00000525456.5:n.500-26T=
ENST00000530052.1:n.395-26T=
ENST00000533687.1:n.483T=
NM_001382.3:c.497-26T=	NP_001373.2:n.497-26T=
XM_005271422.2:c.497-26T=	XP_005271479.1:n.497-26T=
XM_011542648.1:c.176-26T=	XP_011540950.1:n.176-26T=
XR_947801.1:n.933-26T=
XM_005271422.3:c.497-26T=	XP_005271479.1:n.497-26T=
XM_011542648.2:c.176-26T=	XP_011540950.1:n.176-26T=
XM_017017293.2:c.176-26T=	XP_016872782.1:n.176-26T=
XM_017017294.2:c.497-26T=	XP_016872783.1:n.497-26T=
XM_017017295.1:c.-20-26T=	XP_016872784.1:n.-20-26T=
XR_001747785.2:n.720-26T=
XR_947801.2:n.720-26T=
NM_001382.4:c.497-26T= MANE Select	NP_001373.2:n.497-26T=