Canonical Allele Identifier: CA382914134

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119100304-T-C
• MyVariant Identifiers: chr11:g.118971014T>C (hg19) ; chr11:g.119100304T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100304T>C , CM000673.2:g.119100304T>C	GRCh38
NC_000011.9:g.118971014T>C , CM000673.1:g.118971014T>C	GRCh37
NC_000011.8:g.118476224T>C	NCBI36
NG_008918.1:g.6772A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.777A>G
ENST00000530052.2:n.1343A>G
ENST00000682191.1:n.803A>G
ENST00000682192.1:n.803A>G
ENST00000682232.1:c.*306A>G	ENSP00000507302.1:n.*306A>G
ENST00000682326.1:c.601A>G	ENSP00000508129.1:p.Ile201Val
ENST00000682404.1:n.1343A>G
ENST00000682517.1:n.1343A>G
ENST00000682652.1:n.1572A>G
ENST00000682665.1:n.998A>G
ENST00000682691.1:n.998A>G
ENST00000682791.1:c.514A>G	ENSP00000507312.1:p.Ile172Val
ENST00000682811.1:c.601A>G	ENSP00000508196.1:p.Ile201Val
ENST00000682883.1:n.904A>G
ENST00000682946.1:c.601A>G	ENSP00000506856.1:p.Ile201Val
ENST00000683143.1:c.*306A>G	ENSP00000507168.1:n.*306A>G
ENST00000683373.1:n.803A>G
ENST00000683558.1:n.803A>G
ENST00000683567.1:n.828A>G
ENST00000683955.1:n.998A>G
ENST00000684142.1:c.*276A>G	ENSP00000508008.1:n.*276A>G
ENST00000684252.1:n.998A>G
ENST00000684255.1:c.*306A>G	ENSP00000507398.1:n.*306A>G
ENST00000684315.1:n.1334A>G
ENST00000684345.1:c.*276A>G	ENSP00000507163.1:n.*276A>G
ENST00000684499.1:c.*706A>G	ENSP00000506800.1:n.*706A>G
ENST00000684682.1:c.*29A>G	ENSP00000507326.1:n.*29A>G
ENST00000354202.9:c.601A>G MANE Select	ENSP00000346142.4:p.Ile201Val
ENST00000636404.1:c.105A>G
ENST00000638850.1:c.105A>G
ENST00000639704.1:c.508A>G	ENSP00000491336.1:p.Ile170Val
ENST00000640102.1:c.*254A>G	ENSP00000492027.1:n.*254A>G
ENST00000640747.1:c.*276A>G	ENSP00000492730.1:n.*276A>G
ENST00000354202.8:c.601A>G	ENSP00000346142.4:p.Ile201Val
ENST00000392834.7:c.*306A>G	ENSP00000376579.3:n.*306A>G
ENST00000409993.6:c.601A>G	ENSP00000386597.2:p.Ile201Val
ENST00000414373.5:c.*347A>G	ENSP00000402019.1:n.*347A>G
ENST00000442480.1:c.451A>G	ENSP00000406591.1:p.Ile151Val
ENST00000461999.1:n.106A>G
ENST00000481084.5:n.1230A>G
ENST00000525456.5:n.604A>G
ENST00000530052.1:n.499A>G
ENST00000533687.1:n.613A>G
NM_001382.3:c.601A>G	NP_001373.2:p.Ile201Val
XM_005271422.2:c.601A>G	XP_005271479.1:p.Ile201Val
XM_011542648.1:c.280A>G	XP_011540950.1:p.Ile94Val
XR_947801.1:n.1037A>G
XM_005271422.3:c.601A>G	XP_005271479.1:p.Ile201Val
XM_011542648.2:c.280A>G	XP_011540950.1:p.Ile94Val
XM_017017293.2:c.280A>G	XP_016872782.1:p.Ile94Val
XM_017017294.2:c.601A>G	XP_016872783.1:p.Ile201Val
XM_017017295.1:c.85A>G	XP_016872784.1:p.Ile29Val
XR_001747785.2:n.824A>G
XR_947801.2:n.824A>G
NM_001382.4:c.601A>G MANE Select	NP_001373.2:p.Ile201Val