Canonical Allele Identifier: CA382910069

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968257T>C (hg19) ; chr11:g.119097547T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097547T>C , CM000673.2:g.119097547T>C	GRCh38
NC_000011.9:g.118968257T>C , CM000673.1:g.118968257T>C	GRCh37
NC_000011.8:g.118473467T>C	NCBI36
NG_008918.1:g.9529A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.980A>G
ENST00000524658.2:n.961A>G
ENST00000530052.2:n.1967A>G
ENST00000682191.1:n.1427A>G
ENST00000682192.1:n.1124A>G
ENST00000682232.1:c.*623-250A>G	ENSP00000507302.1:n.*623-250A>G
ENST00000682326.1:c.918-250A>G	ENSP00000508129.1:n.918-250A>G
ENST00000682404.1:n.2023A>G
ENST00000682517.1:n.2326A>G
ENST00000682652.1:n.2196A>G
ENST00000682665.1:n.1622A>G
ENST00000682691.1:n.1622A>G
ENST00000682791.1:c.835A>G	ENSP00000507312.1:p.Asn279Asp
ENST00000682811.1:c.804A>G	ENSP00000508196.1:p.Ser268=
ENST00000682883.1:n.1032-250A>G
ENST00000682946.1:c.*4A>G	ENSP00000506856.1:n.*4A>G
ENST00000683143.1:c.*627A>G	ENSP00000507168.1:n.*627A>G
ENST00000683373.1:n.1427A>G
ENST00000683558.1:n.1427A>G
ENST00000683567.1:n.1031A>G
ENST00000683955.1:n.1678A>G
ENST00000684142.1:c.*597A>G	ENSP00000508008.1:n.*597A>G
ENST00000684252.1:n.1319A>G
ENST00000684255.1:c.*627A>G	ENSP00000507398.1:n.*627A>G
ENST00000684315.1:n.1655A>G
ENST00000684345.1:c.*900A>G	ENSP00000507163.1:n.*900A>G
ENST00000684499.1:c.*1027A>G	ENSP00000506800.1:n.*1027A>G
ENST00000684682.1:c.*653A>G	ENSP00000507326.1:n.*653A>G
ENST00000354202.9:c.922A>G MANE Select	ENSP00000346142.4:p.Asn308Asp
ENST00000636404.1:c.233-484A>G
ENST00000638850.1:c.426A>G
ENST00000639704.1:c.829A>G	ENSP00000491336.1:p.Asn277Asp
ENST00000640102.1:c.*575A>G	ENSP00000492027.1:n.*575A>G
ENST00000640747.1:c.*597A>G	ENSP00000492730.1:n.*597A>G
ENST00000354202.8:c.922A>G	ENSP00000346142.4:p.Asn308Asp
ENST00000392834.7:c.*627A>G	ENSP00000376579.3:n.*627A>G
ENST00000409993.6:c.922A>G	ENSP00000386597.2:p.Asn308Asp
ENST00000414373.5:c.*475-250A>G	ENSP00000402019.1:n.*475-250A>G
ENST00000442480.1:c.654A>G	ENSP00000406591.1:p.Ser218=
ENST00000461999.1:n.1089A>G
ENST00000481084.5:n.1551A>G
ENST00000524658.1:n.227A>G
ENST00000525456.5:n.736A>G
NM_001382.3:c.922A>G	NP_001373.2:p.Asn308Asp
XM_005271422.2:c.922A>G	XP_005271479.1:p.Asn308Asp
XM_011542648.1:c.601A>G	XP_011540950.1:p.Asn201Asp
XR_947801.1:n.1165-250A>G
XM_005271422.3:c.922A>G	XP_005271479.1:p.Asn308Asp
XM_011542648.2:c.601A>G	XP_011540950.1:p.Asn201Asp
XM_017017293.2:c.601A>G	XP_016872782.1:p.Asn201Asp
XM_017017294.2:c.*4A>G	XP_016872783.1:n.*4A>G
XM_017017295.1:c.406A>G	XP_016872784.1:p.Asn136Asp
XR_001747785.2:n.956A>G
XR_947801.2:n.952-250A>G
NM_001382.4:c.922A>G MANE Select	NP_001373.2:p.Asn308Asp