Canonical Allele Identifier: CA477140281

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971114G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100404G>T , CM000673.2:g.119100404G>T	GRCh38
NC_000011.9:g.118971114G>T , CM000673.1:g.118971114G>T	GRCh37
NC_000011.8:g.118476324G>T	NCBI36
NG_008918.1:g.6672C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.677C>A
ENST00000530052.2:n.1243C>A
ENST00000682191.1:n.703C>A
ENST00000682192.1:n.703C>A
ENST00000682232.1:c.*206C>A	ENSP00000507302.1:n.*206C>A
ENST00000682326.1:c.501C>A	ENSP00000508129.1:p.Ile167=
ENST00000682404.1:n.1243C>A
ENST00000682517.1:n.1243C>A
ENST00000682652.1:n.1472C>A
ENST00000682665.1:n.898C>A
ENST00000682691.1:n.898C>A
ENST00000682791.1:c.414C>A	ENSP00000507312.1:p.Ile138=
ENST00000682811.1:c.501C>A	ENSP00000508196.1:p.Ile167=
ENST00000682883.1:n.804C>A
ENST00000682946.1:c.501C>A	ENSP00000506856.1:p.Ile167=
ENST00000683143.1:c.*206C>A	ENSP00000507168.1:n.*206C>A
ENST00000683373.1:n.703C>A
ENST00000683558.1:n.703C>A
ENST00000683567.1:n.728C>A
ENST00000683955.1:n.898C>A
ENST00000684142.1:c.*176C>A	ENSP00000508008.1:n.*176C>A
ENST00000684252.1:n.898C>A
ENST00000684255.1:c.*206C>A	ENSP00000507398.1:n.*206C>A
ENST00000684315.1:n.1234C>A
ENST00000684345.1:c.*176C>A	ENSP00000507163.1:n.*176C>A
ENST00000684499.1:c.*606C>A	ENSP00000506800.1:n.*606C>A
ENST00000684682.1:c.166C>A	ENSP00000507326.1:p.Pro56Thr
ENST00000354202.9:c.501C>A MANE Select	ENSP00000346142.4:p.Ile167=
ENST00000636404.1:c.5C>A
ENST00000638850.1:c.5C>A
ENST00000639704.1:c.408C>A	ENSP00000491336.1:p.Ile136=
ENST00000640102.1:c.*154C>A	ENSP00000492027.1:n.*154C>A
ENST00000640747.1:c.*176C>A	ENSP00000492730.1:n.*176C>A
ENST00000354202.8:c.501C>A	ENSP00000346142.4:p.Ile167=
ENST00000392834.7:c.*206C>A	ENSP00000376579.3:n.*206C>A
ENST00000409993.6:c.501C>A	ENSP00000386597.2:p.Ile167=
ENST00000414373.5:c.*247C>A	ENSP00000402019.1:n.*247C>A
ENST00000442480.1:c.351C>A	ENSP00000406591.1:p.Ile117=
ENST00000461999.1:n.6C>A
ENST00000481084.5:n.1130C>A
ENST00000525456.5:n.504C>A
ENST00000530052.1:n.399C>A
ENST00000533687.1:n.513C>A
NM_001382.3:c.501C>A	NP_001373.2:p.Ile167=
XM_005271422.2:c.501C>A	XP_005271479.1:p.Ile167=
XM_011542648.1:c.180C>A	XP_011540950.1:p.Ile60=
XR_947801.1:n.937C>A
XM_005271422.3:c.501C>A	XP_005271479.1:p.Ile167=
XM_011542648.2:c.180C>A	XP_011540950.1:p.Ile60=
XM_017017293.2:c.180C>A	XP_016872782.1:p.Ile60=
XM_017017294.2:c.501C>A	XP_016872783.1:p.Ile167=
XM_017017295.1:c.-16C>A	XP_016872784.1:n.-16C>A
XR_001747785.2:n.724C>A
XR_947801.2:n.724C>A
NM_001382.4:c.501C>A MANE Select	NP_001373.2:p.Ile167=