Canonical Allele Identifier: CA382908173

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097186G>C , CM000673.2:g.119097186G>C	GRCh38
NC_000011.9:g.118967896G>C , CM000673.1:g.118967896G>C	GRCh37
NC_000011.8:g.118473106G>C	NCBI36
NG_008918.1:g.9890C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001382.4:c.1117C>G MANE Select	NP_001373.2:p.Pro373Ala
ENST00000354202.9:c.1117C>G MANE Select	ENSP00000346142.4:p.Pro373Ala
NM_001382.3:c.1117C>G	NP_001373.2:p.Pro373Ala
ENST00000354202.8:c.1117C>G	ENSP00000346142.4:p.Pro373Ala
ENST00000392834.7:c.*822C>G	ENSP00000376579.3:n.*822C>G
ENST00000409993.6:c.1117C>G	ENSP00000386597.2:p.Pro373Ala
ENST00000414373.5:c.*586C>G	ENSP00000402019.1:n.*586C>G
ENST00000442480.1:c.849C>G	ENSP00000406591.1:n.849C>G
ENST00000445653.6:n.1341C>G
ENST00000461999.1:n.1450C>G
ENST00000481084.5:n.1746C>G
ENST00000524658.2:n.1322C>G
ENST00000530052.2:n.2328C>G
ENST00000636404.1:c.233-123C>G
ENST00000638850.1:c.640C>G
ENST00000639704.1:c.1024C>G	ENSP00000491336.1:p.Pro342Ala
ENST00000640102.1:c.*770C>G	ENSP00000492027.1:n.*770C>G
ENST00000640747.1:c.*792C>G	ENSP00000492730.1:n.*792C>G
ENST00000682191.1:n.1622C>G
ENST00000682192.1:n.1485C>G
ENST00000682232.1:c.*734C>G	ENSP00000507302.1:n.*734C>G
ENST00000682326.1:c.*87C>G	ENSP00000508129.1:n.*87C>G
ENST00000682404.1:n.2384C>G
ENST00000682517.1:n.2687C>G
ENST00000682652.1:n.2391C>G
ENST00000682665.1:n.1983C>G
ENST00000682691.1:n.1983C>G
ENST00000682791.1:c.1030C>G	ENSP00000507312.1:p.Pro344Ala
ENST00000682811.1:c.*168C>G	ENSP00000508196.1:n.*168C>G
ENST00000682883.1:n.1143C>G
ENST00000682946.1:c.*199C>G	ENSP00000506856.1:n.*199C>G
ENST00000683143.1:c.*822C>G	ENSP00000507168.1:n.*822C>G
ENST00000683373.1:n.1622C>G
ENST00000683558.1:n.1788C>G
ENST00000683567.1:n.1226C>G
ENST00000683955.1:n.1873C>G
ENST00000684142.1:c.*958C>G	ENSP00000508008.1:n.*958C>G
ENST00000684252.1:n.1680C>G
ENST00000684255.1:c.*988C>G	ENSP00000507398.1:n.*988C>G
ENST00000684315.1:n.1850C>G
ENST00000684345.1:c.*1261C>G	ENSP00000507163.1:n.*1261C>G
ENST00000684499.1:c.*1388C>G	ENSP00000506800.1:n.*1388C>G
ENST00000684682.1:c.*1014C>G	ENSP00000507326.1:n.*1014C>G
XM_005271422.2:c.1117C>G	XP_005271479.1:p.Pro373Ala
XM_005271422.3:c.1117C>G	XP_005271479.1:p.Pro373Ala
XM_011542648.1:c.796C>G	XP_011540950.1:p.Pro266Ala
XM_011542648.2:c.796C>G	XP_011540950.1:p.Pro266Ala
XM_017017293.2:c.796C>G	XP_016872782.1:p.Pro266Ala
XM_017017294.2:c.*365C>G	XP_016872783.1:n.*365C>G
XM_017017295.1:c.601C>G	XP_016872784.1:p.Pro201Ala
XR_001747785.2:n.1151C>G
XR_947801.1:n.1276C>G
XR_947801.2:n.1063C>G