Canonical Allele Identifier: CA1619828519
Community Standard Title: NM_002119.4(HLA-DOA):c.82+578C=
Gene: HLA-DOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33008877G= , CM000668.2:g.33008877G= GRCh38
NC_000006.11:g.32976654G= , CM000668.1:g.32976654G= GRCh37
NC_000006.10:g.33084632G= NCBI36
NG_012007.1:g.5736C=

Transcript Alleles

HGVS Amino-acid Change
NM_002119.4:c.82+578C= MANE Select NP_002110.1:n.82+578C=
ENST00000229829.7:c.82+578C= MANE Select ENSP00000229829.3:n.82+578C=
NM_002119.3:c.82+578C= NP_002110.1:n.82+578C=
ENST00000229829.6:c.82+578C= ENSP00000229829.3:n.82+578C=
ENST00000374813.1:c.82+578C= ENSP00000363946.1:n.82+578C=
ENST00000450833.3:c.82+578C= ENSP00000403896.3:n.82+578C=
ENST00000467465.1:n.129-473C=
XM_005249047.3:c.82+578C= XP_005249104.1:n.82+578C=
XM_006715076.2:c.-151-473C= XP_006715139.1:n.-151-473C=
XM_011514558.1:c.82+578C= XP_011512860.1:n.82+578C=