Canonical Allele Identifier: CA382915337

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971512C>T (hg19) ; chr11:g.119100802C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100802C>T , CM000673.2:g.119100802C>T	GRCh38
NC_000011.9:g.118971512C>T , CM000673.1:g.118971512C>T	GRCh37
NC_000011.8:g.118476722C>T	NCBI36
NG_008918.1:g.6274G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.500G>A
ENST00000530052.2:n.1066G>A
ENST00000682191.1:n.526G>A
ENST00000682192.1:n.526G>A
ENST00000682232.1:c.*29G>A	ENSP00000507302.1:n.*29G>A
ENST00000682326.1:c.324G>A	ENSP00000508129.1:p.Met108Ile
ENST00000682404.1:n.1066G>A
ENST00000682517.1:n.1066G>A
ENST00000682652.1:n.1295G>A
ENST00000682665.1:n.721G>A
ENST00000682691.1:n.721G>A
ENST00000682791.1:c.237G>A	ENSP00000507312.1:p.Met79Ile
ENST00000682811.1:c.324G>A	ENSP00000508196.1:p.Met108Ile
ENST00000682883.1:n.627G>A
ENST00000682946.1:c.324G>A	ENSP00000506856.1:p.Met108Ile
ENST00000683143.1:c.*29G>A	ENSP00000507168.1:n.*29G>A
ENST00000683373.1:n.526G>A
ENST00000683558.1:n.526G>A
ENST00000683567.1:n.551G>A
ENST00000683955.1:n.721G>A
ENST00000684142.1:c.308G>A	ENSP00000508008.1:p.Ter103=
ENST00000684252.1:n.721G>A
ENST00000684255.1:c.*29G>A	ENSP00000507398.1:n.*29G>A
ENST00000684315.1:n.1057G>A
ENST00000684345.1:c.308G>A	ENSP00000507163.1:p.Ter103=
ENST00000684499.1:c.*429G>A	ENSP00000506800.1:n.*429G>A
ENST00000684682.1:c.162-394G>A	ENSP00000507326.1:n.162-394G>A
ENST00000354202.9:c.324G>A MANE Select	ENSP00000346142.4:p.Met108Ile
ENST00000639704.1:c.283-52G>A	ENSP00000491336.1:n.283-52G>A
ENST00000640102.1:c.187G>A	ENSP00000492027.1:p.Asp63Asn
ENST00000640747.1:c.308G>A	ENSP00000492730.1:p.Ter103=
ENST00000354202.8:c.324G>A	ENSP00000346142.4:p.Met108Ile
ENST00000392834.7:c.*29G>A	ENSP00000376579.3:n.*29G>A
ENST00000409993.6:c.324G>A	ENSP00000386597.2:p.Met108Ile
ENST00000414373.5:c.*70G>A	ENSP00000402019.1:n.*70G>A
ENST00000442480.1:c.174G>A	ENSP00000406591.1:p.Met58Ile
ENST00000445653.5:n.410G>A
ENST00000460183.1:n.885G>A
ENST00000481084.5:n.1125+216G>A
ENST00000525456.5:n.327G>A
ENST00000530052.1:n.222G>A
ENST00000533687.1:n.115G>A
NM_001382.3:c.324G>A	NP_001373.2:p.Met108Ile
XM_005271422.2:c.324G>A	XP_005271479.1:p.Met108Ile
XM_011542648.1:c.3G>A	XP_011540950.1:p.Met1Ile
XR_947801.1:n.760G>A
XM_005271422.3:c.324G>A	XP_005271479.1:p.Met108Ile
XM_011542648.2:c.3G>A	XP_011540950.1:p.Met1Ile
XM_017017293.2:c.3G>A	XP_016872782.1:p.Met1Ile
XM_017017294.2:c.324G>A	XP_016872783.1:p.Met108Ile
XM_017017295.1:c.-20-394G>A	XP_016872784.1:n.-20-394G>A
XR_001747785.2:n.547G>A
XR_947801.2:n.547G>A
NM_001382.4:c.324G>A MANE Select	NP_001373.2:p.Met108Ile