Canonical Allele Identifier: CA382910027

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968247G>C (hg19) ; chr11:g.119097537G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097537G>C , CM000673.2:g.119097537G>C	GRCh38
NC_000011.9:g.118968247G>C , CM000673.1:g.118968247G>C	GRCh37
NC_000011.8:g.118473457G>C	NCBI36
NG_008918.1:g.9539C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.990C>G
ENST00000524658.2:n.971C>G
ENST00000530052.2:n.1977C>G
ENST00000682191.1:n.1437C>G
ENST00000682192.1:n.1134C>G
ENST00000682232.1:c.*623-240C>G	ENSP00000507302.1:n.*623-240C>G
ENST00000682326.1:c.918-240C>G	ENSP00000508129.1:n.918-240C>G
ENST00000682404.1:n.2033C>G
ENST00000682517.1:n.2336C>G
ENST00000682652.1:n.2206C>G
ENST00000682665.1:n.1632C>G
ENST00000682691.1:n.1632C>G
ENST00000682791.1:c.845C>G	ENSP00000507312.1:p.Thr282Arg
ENST00000682811.1:c.814C>G	ENSP00000508196.1:p.Gln272Glu
ENST00000682883.1:n.1032-240C>G
ENST00000682946.1:c.*14C>G	ENSP00000506856.1:n.*14C>G
ENST00000683143.1:c.*637C>G	ENSP00000507168.1:n.*637C>G
ENST00000683373.1:n.1437C>G
ENST00000683558.1:n.1437C>G
ENST00000683567.1:n.1041C>G
ENST00000683955.1:n.1688C>G
ENST00000684142.1:c.*607C>G	ENSP00000508008.1:n.*607C>G
ENST00000684252.1:n.1329C>G
ENST00000684255.1:c.*637C>G	ENSP00000507398.1:n.*637C>G
ENST00000684315.1:n.1665C>G
ENST00000684345.1:c.*910C>G	ENSP00000507163.1:n.*910C>G
ENST00000684499.1:c.*1037C>G	ENSP00000506800.1:n.*1037C>G
ENST00000684682.1:c.*663C>G	ENSP00000507326.1:n.*663C>G
ENST00000354202.9:c.932C>G MANE Select	ENSP00000346142.4:p.Thr311Arg
ENST00000636404.1:c.233-474C>G
ENST00000638850.1:c.436C>G
ENST00000639704.1:c.839C>G	ENSP00000491336.1:p.Thr280Arg
ENST00000640102.1:c.*585C>G	ENSP00000492027.1:n.*585C>G
ENST00000640747.1:c.*607C>G	ENSP00000492730.1:n.*607C>G
ENST00000354202.8:c.932C>G	ENSP00000346142.4:p.Thr311Arg
ENST00000392834.7:c.*637C>G	ENSP00000376579.3:n.*637C>G
ENST00000409993.6:c.932C>G	ENSP00000386597.2:p.Thr311Arg
ENST00000414373.5:c.*475-240C>G	ENSP00000402019.1:n.*475-240C>G
ENST00000442480.1:c.664C>G	ENSP00000406591.1:p.Gln222Glu
ENST00000461999.1:n.1099C>G
ENST00000481084.5:n.1561C>G
ENST00000524658.1:n.237C>G
ENST00000525456.5:n.746C>G
NM_001382.3:c.932C>G	NP_001373.2:p.Thr311Arg
XM_005271422.2:c.932C>G	XP_005271479.1:p.Thr311Arg
XM_011542648.1:c.611C>G	XP_011540950.1:p.Thr204Arg
XR_947801.1:n.1165-240C>G
XM_005271422.3:c.932C>G	XP_005271479.1:p.Thr311Arg
XM_011542648.2:c.611C>G	XP_011540950.1:p.Thr204Arg
XM_017017293.2:c.611C>G	XP_016872782.1:p.Thr204Arg
XM_017017294.2:c.*14C>G	XP_016872783.1:n.*14C>G
XM_017017295.1:c.416C>G	XP_016872784.1:p.Thr139Arg
XR_001747785.2:n.966C>G
XR_947801.2:n.952-240C>G
NM_001382.4:c.932C>G MANE Select	NP_001373.2:p.Thr311Arg