Canonical Allele Identifier: CA382914889

Gene: DPAGT1

Linked Data

• COSMIC: COSM3935340
• MyVariant Identifiers: chr11:g.118971118C>A (hg19) ; chr11:g.119100408C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100408C>A , CM000673.2:g.119100408C>A	GRCh38
NC_000011.9:g.118971118C>A , CM000673.1:g.118971118C>A	GRCh37
NC_000011.8:g.118476328C>A	NCBI36
NG_008918.1:g.6668G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.673G>T
ENST00000530052.2:n.1239G>T
ENST00000682191.1:n.699G>T
ENST00000682192.1:n.699G>T
ENST00000682232.1:c.*202G>T	ENSP00000507302.1:n.*202G>T
ENST00000682326.1:c.497G>T	ENSP00000508129.1:p.Gly166Val
ENST00000682404.1:n.1239G>T
ENST00000682517.1:n.1239G>T
ENST00000682652.1:n.1468G>T
ENST00000682665.1:n.894G>T
ENST00000682691.1:n.894G>T
ENST00000682791.1:c.410G>T	ENSP00000507312.1:p.Gly137Val
ENST00000682811.1:c.497G>T	ENSP00000508196.1:p.Gly166Val
ENST00000682883.1:n.800G>T
ENST00000682946.1:c.497G>T	ENSP00000506856.1:p.Gly166Val
ENST00000683143.1:c.*202G>T	ENSP00000507168.1:n.*202G>T
ENST00000683373.1:n.699G>T
ENST00000683558.1:n.699G>T
ENST00000683567.1:n.724G>T
ENST00000683955.1:n.894G>T
ENST00000684142.1:c.*172G>T	ENSP00000508008.1:n.*172G>T
ENST00000684252.1:n.894G>T
ENST00000684255.1:c.*202G>T	ENSP00000507398.1:n.*202G>T
ENST00000684315.1:n.1230G>T
ENST00000684345.1:c.*172G>T	ENSP00000507163.1:n.*172G>T
ENST00000684499.1:c.*602G>T	ENSP00000506800.1:n.*602G>T
ENST00000684682.1:c.162G>T	ENSP00000507326.1:p.Met54Ile
ENST00000354202.9:c.497G>T MANE Select	ENSP00000346142.4:p.Gly166Val
ENST00000636404.1:c.1G>T
ENST00000638850.1:c.1G>T
ENST00000639704.1:c.404G>T	ENSP00000491336.1:p.Gly135Val
ENST00000640102.1:c.*150G>T	ENSP00000492027.1:n.*150G>T
ENST00000640747.1:c.*172G>T	ENSP00000492730.1:n.*172G>T
ENST00000354202.8:c.497G>T	ENSP00000346142.4:p.Gly166Val
ENST00000392834.7:c.*202G>T	ENSP00000376579.3:n.*202G>T
ENST00000409993.6:c.497G>T	ENSP00000386597.2:p.Gly166Val
ENST00000414373.5:c.*243G>T	ENSP00000402019.1:n.*243G>T
ENST00000442480.1:c.347G>T	ENSP00000406591.1:p.Gly116Val
ENST00000461999.1:n.2G>T
ENST00000481084.5:n.1126G>T
ENST00000525456.5:n.500G>T
ENST00000530052.1:n.395G>T
ENST00000533687.1:n.509G>T
NM_001382.3:c.497G>T	NP_001373.2:p.Gly166Val
XM_005271422.2:c.497G>T	XP_005271479.1:p.Gly166Val
XM_011542648.1:c.176G>T	XP_011540950.1:p.Gly59Val
XR_947801.1:n.933G>T
XM_005271422.3:c.497G>T	XP_005271479.1:p.Gly166Val
XM_011542648.2:c.176G>T	XP_011540950.1:p.Gly59Val
XM_017017293.2:c.176G>T	XP_016872782.1:p.Gly59Val
XM_017017294.2:c.497G>T	XP_016872783.1:p.Gly166Val
XM_017017295.1:c.-20G>T	XP_016872784.1:n.-20G>T
XR_001747785.2:n.720G>T
XR_947801.2:n.720G>T
NM_001382.4:c.497G>T MANE Select	NP_001373.2:p.Gly166Val