Canonical Allele Identifier: CA2580601008

Gene: DPAGT1

Genomic Alleles

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

Transcript Alleles

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