Canonical Allele Identifier: CA382909552

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968193A>G (hg19) ; chr11:g.119097483A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097483A>G , CM000673.2:g.119097483A>G	GRCh38
NC_000011.9:g.118968193A>G , CM000673.1:g.118968193A>G	GRCh37
NC_000011.8:g.118473403A>G	NCBI36
NG_008918.1:g.9593T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1044T>C
ENST00000524658.2:n.1025T>C
ENST00000530052.2:n.2031T>C
ENST00000682191.1:n.1491T>C
ENST00000682192.1:n.1188T>C
ENST00000682232.1:c.*623-186T>C	ENSP00000507302.1:n.*623-186T>C
ENST00000682326.1:c.918-186T>C	ENSP00000508129.1:n.918-186T>C
ENST00000682404.1:n.2087T>C
ENST00000682517.1:n.2390T>C
ENST00000682652.1:n.2260T>C
ENST00000682665.1:n.1686T>C
ENST00000682691.1:n.1686T>C
ENST00000682791.1:c.899T>C	ENSP00000507312.1:p.Leu300Ser
ENST00000682811.1:c.*37T>C	ENSP00000508196.1:n.*37T>C
ENST00000682883.1:n.1032-186T>C
ENST00000682946.1:c.*68T>C	ENSP00000506856.1:n.*68T>C
ENST00000683143.1:c.*691T>C	ENSP00000507168.1:n.*691T>C
ENST00000683373.1:n.1491T>C
ENST00000683558.1:n.1491T>C
ENST00000683567.1:n.1095T>C
ENST00000683955.1:n.1742T>C
ENST00000684142.1:c.*661T>C	ENSP00000508008.1:n.*661T>C
ENST00000684252.1:n.1383T>C
ENST00000684255.1:c.*691T>C	ENSP00000507398.1:n.*691T>C
ENST00000684315.1:n.1719T>C
ENST00000684345.1:c.*964T>C	ENSP00000507163.1:n.*964T>C
ENST00000684499.1:c.*1091T>C	ENSP00000506800.1:n.*1091T>C
ENST00000684682.1:c.*717T>C	ENSP00000507326.1:n.*717T>C
ENST00000354202.9:c.986T>C MANE Select	ENSP00000346142.4:p.Leu329Ser
ENST00000636404.1:c.233-420T>C
ENST00000638850.1:c.490T>C
ENST00000639704.1:c.893T>C	ENSP00000491336.1:p.Leu298Ser
ENST00000640102.1:c.*639T>C	ENSP00000492027.1:n.*639T>C
ENST00000640747.1:c.*661T>C	ENSP00000492730.1:n.*661T>C
ENST00000354202.8:c.986T>C	ENSP00000346142.4:p.Leu329Ser
ENST00000392834.7:c.*691T>C	ENSP00000376579.3:n.*691T>C
ENST00000409993.6:c.986T>C	ENSP00000386597.2:p.Leu329Ser
ENST00000414373.5:c.*475-186T>C	ENSP00000402019.1:n.*475-186T>C
ENST00000442480.1:c.718T>C	ENSP00000406591.1:n.718T>C
ENST00000461999.1:n.1153T>C
ENST00000481084.5:n.1615T>C
ENST00000524658.1:n.291T>C
ENST00000525456.5:n.800T>C
NM_001382.3:c.986T>C	NP_001373.2:p.Leu329Ser
XM_005271422.2:c.986T>C	XP_005271479.1:p.Leu329Ser
XM_011542648.1:c.665T>C	XP_011540950.1:p.Leu222Ser
XR_947801.1:n.1165-186T>C
XM_005271422.3:c.986T>C	XP_005271479.1:p.Leu329Ser
XM_011542648.2:c.665T>C	XP_011540950.1:p.Leu222Ser
XM_017017293.2:c.665T>C	XP_016872782.1:p.Leu222Ser
XM_017017294.2:c.*68T>C	XP_016872783.1:n.*68T>C
XM_017017295.1:c.470T>C	XP_016872784.1:p.Leu157Ser
XR_001747785.2:n.1020T>C
XR_947801.2:n.952-186T>C
NM_001382.4:c.986T>C MANE Select	NP_001373.2:p.Leu329Ser