Canonical Allele Identifier: CA382907423

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097028A>T , CM000673.2:g.119097028A>T	GRCh38
NC_000011.9:g.118967738A>T , CM000673.1:g.118967738A>T	GRCh37
NC_000011.8:g.118472948A>T	NCBI36
NG_008918.1:g.10048T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001382.4:c.1197T>A MANE Select	NP_001373.2:p.Tyr399Ter
ENST00000354202.9:c.1197T>A MANE Select	ENSP00000346142.4:p.Tyr399Ter
NM_001382.3:c.1197T>A	NP_001373.2:p.Tyr399Ter
ENST00000354202.8:c.1197T>A	ENSP00000346142.4:p.Tyr399Ter
ENST00000392834.7:c.*902T>A	ENSP00000376579.3:n.*902T>A
ENST00000409993.6:c.1197T>A	ENSP00000386597.2:p.Tyr399Ter
ENST00000414373.5:c.*666T>A	ENSP00000402019.1:n.*666T>A
ENST00000442480.1:c.929T>A	ENSP00000406591.1:n.929T>A
ENST00000445653.6:n.1421T>A
ENST00000461999.1:n.1608T>A
ENST00000481084.5:n.1826T>A
ENST00000524658.2:n.1480T>A
ENST00000530052.2:n.2486T>A
ENST00000636404.1:c.268T>A
ENST00000638850.1:c.720T>A
ENST00000639704.1:c.1104T>A	ENSP00000491336.1:p.Tyr368Ter
ENST00000640747.1:c.*872T>A	ENSP00000492730.1:n.*872T>A
ENST00000682191.1:n.1780T>A
ENST00000682192.1:n.1643T>A
ENST00000682232.1:c.*814T>A	ENSP00000507302.1:n.*814T>A
ENST00000682326.1:c.*167T>A	ENSP00000508129.1:n.*167T>A
ENST00000682404.1:n.2542T>A
ENST00000682517.1:n.2767T>A
ENST00000682652.1:n.2549T>A
ENST00000682665.1:n.2141T>A
ENST00000682691.1:n.2063T>A
ENST00000682791.1:c.1110T>A	ENSP00000507312.1:p.Tyr370Ter
ENST00000682811.1:c.*248T>A	ENSP00000508196.1:n.*248T>A
ENST00000682883.1:n.1301T>A
ENST00000682946.1:c.*279T>A	ENSP00000506856.1:n.*279T>A
ENST00000683143.1:c.*902T>A	ENSP00000507168.1:n.*902T>A
ENST00000683373.1:n.1702T>A
ENST00000683558.1:n.1946T>A
ENST00000683567.1:n.1306T>A
ENST00000683955.1:n.1953T>A
ENST00000684142.1:c.*1038T>A	ENSP00000508008.1:n.*1038T>A
ENST00000684252.1:n.1838T>A
ENST00000684255.1:c.*1068T>A	ENSP00000507398.1:n.*1068T>A
ENST00000684315.1:n.2008T>A
ENST00000684345.1:c.*1341T>A	ENSP00000507163.1:n.*1341T>A
ENST00000684499.1:c.*1468T>A	ENSP00000506800.1:n.*1468T>A
ENST00000684682.1:c.*1172T>A	ENSP00000507326.1:n.*1172T>A
XM_005271422.2:c.1275T>A	XP_005271479.1:p.Tyr425Ter
XM_005271422.3:c.1275T>A	XP_005271479.1:p.Tyr425Ter
XM_011542648.1:c.954T>A	XP_011540950.1:p.Tyr318Ter
XM_011542648.2:c.954T>A	XP_011540950.1:p.Tyr318Ter
XM_017017293.2:c.876T>A	XP_016872782.1:p.Tyr292Ter
XM_017017294.2:c.*523T>A	XP_016872783.1:n.*523T>A
XM_017017295.1:c.681T>A	XP_016872784.1:p.Tyr227Ter
XR_001747785.2:n.1231T>A
XR_947801.1:n.1356T>A
XR_947801.2:n.1143T>A