Canonical Allele Identifier: CA382909931

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968224A>T (hg19) ; chr11:g.119097514A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097514A>T , CM000673.2:g.119097514A>T	GRCh38
NC_000011.9:g.118968224A>T , CM000673.1:g.118968224A>T	GRCh37
NC_000011.8:g.118473434A>T	NCBI36
NG_008918.1:g.9562T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1013T>A
ENST00000524658.2:n.994T>A
ENST00000530052.2:n.2000T>A
ENST00000682191.1:n.1460T>A
ENST00000682192.1:n.1157T>A
ENST00000682232.1:c.*623-217T>A	ENSP00000507302.1:n.*623-217T>A
ENST00000682326.1:c.918-217T>A	ENSP00000508129.1:n.918-217T>A
ENST00000682404.1:n.2056T>A
ENST00000682517.1:n.2359T>A
ENST00000682652.1:n.2229T>A
ENST00000682665.1:n.1655T>A
ENST00000682691.1:n.1655T>A
ENST00000682791.1:c.868T>A	ENSP00000507312.1:p.Ser290Thr
ENST00000682811.1:c.*6T>A	ENSP00000508196.1:n.*6T>A
ENST00000682883.1:n.1032-217T>A
ENST00000682946.1:c.*37T>A	ENSP00000506856.1:n.*37T>A
ENST00000683143.1:c.*660T>A	ENSP00000507168.1:n.*660T>A
ENST00000683373.1:n.1460T>A
ENST00000683558.1:n.1460T>A
ENST00000683567.1:n.1064T>A
ENST00000683955.1:n.1711T>A
ENST00000684142.1:c.*630T>A	ENSP00000508008.1:n.*630T>A
ENST00000684252.1:n.1352T>A
ENST00000684255.1:c.*660T>A	ENSP00000507398.1:n.*660T>A
ENST00000684315.1:n.1688T>A
ENST00000684345.1:c.*933T>A	ENSP00000507163.1:n.*933T>A
ENST00000684499.1:c.*1060T>A	ENSP00000506800.1:n.*1060T>A
ENST00000684682.1:c.*686T>A	ENSP00000507326.1:n.*686T>A
ENST00000354202.9:c.955T>A MANE Select	ENSP00000346142.4:p.Ser319Thr
ENST00000636404.1:c.233-451T>A
ENST00000638850.1:c.459T>A
ENST00000639704.1:c.862T>A	ENSP00000491336.1:p.Ser288Thr
ENST00000640102.1:c.*608T>A	ENSP00000492027.1:n.*608T>A
ENST00000640747.1:c.*630T>A	ENSP00000492730.1:n.*630T>A
ENST00000354202.8:c.955T>A	ENSP00000346142.4:p.Ser319Thr
ENST00000392834.7:c.*660T>A	ENSP00000376579.3:n.*660T>A
ENST00000409993.6:c.955T>A	ENSP00000386597.2:p.Ser319Thr
ENST00000414373.5:c.*475-217T>A	ENSP00000402019.1:n.*475-217T>A
ENST00000442480.1:c.687T>A	ENSP00000406591.1:n.687T>A
ENST00000461999.1:n.1122T>A
ENST00000481084.5:n.1584T>A
ENST00000524658.1:n.260T>A
ENST00000525456.5:n.769T>A
NM_001382.3:c.955T>A	NP_001373.2:p.Ser319Thr
XM_005271422.2:c.955T>A	XP_005271479.1:p.Ser319Thr
XM_011542648.1:c.634T>A	XP_011540950.1:p.Ser212Thr
XR_947801.1:n.1165-217T>A
XM_005271422.3:c.955T>A	XP_005271479.1:p.Ser319Thr
XM_011542648.2:c.634T>A	XP_011540950.1:p.Ser212Thr
XM_017017293.2:c.634T>A	XP_016872782.1:p.Ser212Thr
XM_017017294.2:c.*37T>A	XP_016872783.1:n.*37T>A
XM_017017295.1:c.439T>A	XP_016872784.1:p.Ser147Thr
XR_001747785.2:n.989T>A
XR_947801.2:n.952-217T>A
NM_001382.4:c.955T>A MANE Select	NP_001373.2:p.Ser319Thr