Canonical Allele Identifier: CA382914122

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971013A>G (hg19) ; chr11:g.119100303A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100303A>G , CM000673.2:g.119100303A>G	GRCh38
NC_000011.9:g.118971013A>G , CM000673.1:g.118971013A>G	GRCh37
NC_000011.8:g.118476223A>G	NCBI36
NG_008918.1:g.6773T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000445653.6:n.778T>C
ENST00000530052.2:n.1344T>C
ENST00000682191.1:n.804T>C
ENST00000682192.1:n.804T>C
ENST00000682232.1:c.*307T>C	ENSP00000507302.1:n.*307T>C
ENST00000682326.1:c.602T>C	ENSP00000508129.1:p.Ile201Thr
ENST00000682404.1:n.1344T>C
ENST00000682517.1:n.1344T>C
ENST00000682652.1:n.1573T>C
ENST00000682665.1:n.999T>C
ENST00000682691.1:n.999T>C
ENST00000682791.1:c.515T>C	ENSP00000507312.1:p.Ile172Thr
ENST00000682811.1:c.602T>C	ENSP00000508196.1:p.Ile201Thr
ENST00000682883.1:n.905T>C
ENST00000682946.1:c.602T>C	ENSP00000506856.1:p.Ile201Thr
ENST00000683143.1:c.*307T>C	ENSP00000507168.1:n.*307T>C
ENST00000683373.1:n.804T>C
ENST00000683558.1:n.804T>C
ENST00000683567.1:n.829T>C
ENST00000683955.1:n.999T>C
ENST00000684142.1:c.*277T>C	ENSP00000508008.1:n.*277T>C
ENST00000684252.1:n.999T>C
ENST00000684255.1:c.*307T>C	ENSP00000507398.1:n.*307T>C
ENST00000684315.1:n.1335T>C
ENST00000684345.1:c.*277T>C	ENSP00000507163.1:n.*277T>C
ENST00000684499.1:c.*707T>C	ENSP00000506800.1:n.*707T>C
ENST00000684682.1:c.*30T>C	ENSP00000507326.1:n.*30T>C
ENST00000354202.9:c.602T>C MANE Select	ENSP00000346142.4:p.Ile201Thr
ENST00000636404.1:c.106T>C
ENST00000638850.1:c.106T>C
ENST00000639704.1:c.509T>C	ENSP00000491336.1:p.Ile170Thr
ENST00000640102.1:c.*255T>C	ENSP00000492027.1:n.*255T>C
ENST00000640747.1:c.*277T>C	ENSP00000492730.1:n.*277T>C
ENST00000354202.8:c.602T>C	ENSP00000346142.4:p.Ile201Thr
ENST00000392834.7:c.*307T>C	ENSP00000376579.3:n.*307T>C
ENST00000409993.6:c.602T>C	ENSP00000386597.2:p.Ile201Thr
ENST00000414373.5:c.*348T>C	ENSP00000402019.1:n.*348T>C
ENST00000442480.1:c.452T>C	ENSP00000406591.1:p.Ile151Thr
ENST00000461999.1:n.107T>C
ENST00000481084.5:n.1231T>C
ENST00000525456.5:n.605T>C
ENST00000530052.1:n.500T>C
ENST00000533687.1:n.614T>C
NM_001382.3:c.602T>C	NP_001373.2:p.Ile201Thr
XM_005271422.2:c.602T>C	XP_005271479.1:p.Ile201Thr
XM_011542648.1:c.281T>C	XP_011540950.1:p.Ile94Thr
XR_947801.1:n.1038T>C
XM_005271422.3:c.602T>C	XP_005271479.1:p.Ile201Thr
XM_011542648.2:c.281T>C	XP_011540950.1:p.Ile94Thr
XM_017017293.2:c.281T>C	XP_016872782.1:p.Ile94Thr
XM_017017294.2:c.602T>C	XP_016872783.1:p.Ile201Thr
XM_017017295.1:c.86T>C	XP_016872784.1:p.Ile29Thr
XR_001747785.2:n.825T>C
XR_947801.2:n.825T>C
NM_001382.4:c.602T>C MANE Select	NP_001373.2:p.Ile201Thr