Canonical Allele Identifier: CA382914837

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971109T>A (hg19) ; chr11:g.119100399T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100399T>A , CM000673.2:g.119100399T>A	GRCh38
NC_000011.9:g.118971109T>A , CM000673.1:g.118971109T>A	GRCh37
NC_000011.8:g.118476319T>A	NCBI36
NG_008918.1:g.6677A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.682A>T
ENST00000530052.2:n.1248A>T
ENST00000682191.1:n.708A>T
ENST00000682192.1:n.708A>T
ENST00000682232.1:c.*211A>T	ENSP00000507302.1:n.*211A>T
ENST00000682326.1:c.506A>T	ENSP00000508129.1:p.Tyr169Phe
ENST00000682404.1:n.1248A>T
ENST00000682517.1:n.1248A>T
ENST00000682652.1:n.1477A>T
ENST00000682665.1:n.903A>T
ENST00000682691.1:n.903A>T
ENST00000682791.1:c.419A>T	ENSP00000507312.1:p.Tyr140Phe
ENST00000682811.1:c.506A>T	ENSP00000508196.1:p.Tyr169Phe
ENST00000682883.1:n.809A>T
ENST00000682946.1:c.506A>T	ENSP00000506856.1:p.Tyr169Phe
ENST00000683143.1:c.*211A>T	ENSP00000507168.1:n.*211A>T
ENST00000683373.1:n.708A>T
ENST00000683558.1:n.708A>T
ENST00000683567.1:n.733A>T
ENST00000683955.1:n.903A>T
ENST00000684142.1:c.*181A>T	ENSP00000508008.1:n.*181A>T
ENST00000684252.1:n.903A>T
ENST00000684255.1:c.*211A>T	ENSP00000507398.1:n.*211A>T
ENST00000684315.1:n.1239A>T
ENST00000684345.1:c.*181A>T	ENSP00000507163.1:n.*181A>T
ENST00000684499.1:c.*611A>T	ENSP00000506800.1:n.*611A>T
ENST00000684682.1:c.171A>T	ENSP00000507326.1:p.Val57=
ENST00000354202.9:c.506A>T MANE Select	ENSP00000346142.4:p.Tyr169Phe
ENST00000636404.1:c.10A>T
ENST00000638850.1:c.10A>T
ENST00000639704.1:c.413A>T	ENSP00000491336.1:p.Tyr138Phe
ENST00000640102.1:c.*159A>T	ENSP00000492027.1:n.*159A>T
ENST00000640747.1:c.*181A>T	ENSP00000492730.1:n.*181A>T
ENST00000354202.8:c.506A>T	ENSP00000346142.4:p.Tyr169Phe
ENST00000392834.7:c.*211A>T	ENSP00000376579.3:n.*211A>T
ENST00000409993.6:c.506A>T	ENSP00000386597.2:p.Tyr169Phe
ENST00000414373.5:c.*252A>T	ENSP00000402019.1:n.*252A>T
ENST00000442480.1:c.356A>T	ENSP00000406591.1:p.Tyr119Phe
ENST00000461999.1:n.11A>T
ENST00000481084.5:n.1135A>T
ENST00000525456.5:n.509A>T
ENST00000530052.1:n.404A>T
ENST00000533687.1:n.518A>T
NM_001382.3:c.506A>T	NP_001373.2:p.Tyr169Phe
XM_005271422.2:c.506A>T	XP_005271479.1:p.Tyr169Phe
XM_011542648.1:c.185A>T	XP_011540950.1:p.Tyr62Phe
XR_947801.1:n.942A>T
XM_005271422.3:c.506A>T	XP_005271479.1:p.Tyr169Phe
XM_011542648.2:c.185A>T	XP_011540950.1:p.Tyr62Phe
XM_017017293.2:c.185A>T	XP_016872782.1:p.Tyr62Phe
XM_017017294.2:c.506A>T	XP_016872783.1:p.Tyr169Phe
XM_017017295.1:c.-11A>T	XP_016872784.1:n.-11A>T
XR_001747785.2:n.729A>T
XR_947801.2:n.729A>T
NM_001382.4:c.506A>T MANE Select	NP_001373.2:p.Tyr169Phe