Canonical Allele Identifier: CA449831170
Gene: HLA-DQA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32609972G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32642195G>A , CM000668.2:g.32642195G>A GRCh38
NC_000006.11:g.32609972G>A , CM000668.1:g.32609972G>A GRCh37
NC_000006.10:g.32717950G>A NCBI36
NG_032876.1:g.9790G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343139.11:c.555G>A MANE Select ENSP00000339398.5:p.Glu185=
ENST00000343139.9:c.555G>A ENSP00000339398.5:p.Glu185=
ENST00000374949.2:c.555G>A ENSP00000364087.2:p.Glu185=
ENST00000395363.5:c.555G>A ENSP00000378767.1:p.Glu185=
ENST00000460633.1:n.583G>A
ENST00000482745.5:c.*1387G>A ENSP00000436546.1:n.*1387G>A
ENST00000496318.5:c.555G>A ENSP00000437302.1:p.Glu185=
NM_002122.3:c.555G>A NP_002113.2:p.Glu185=
XM_006715079.2:c.555G>A XP_006715142.1:p.Glu185=
XM_006715079.4:c.555G>A XP_006715142.1:p.Glu185=
XR_001744085.1:n.86+393C>T
NM_002122.5:c.555G>A MANE Select NP_002113.2:p.Glu185=