Canonical Allele Identifier: CA512490981
Gene: AIRE HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45709625C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44289742C>G , CM000683.2:g.44289742C>G GRCh38
NC_000021.8:g.45709625C>G , CM000683.1:g.45709625C>G GRCh37
NC_000021.7:g.44534053C>G NCBI36
NG_009556.1:g.8863C>G , LRG_18:g.8863C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.738C>G MANE Select ENSP00000291582.5:p.Ala246=
ENST00000291582.5:c.738C>G ENSP00000291582.5:p.Ala246=
ENST00000527919.5:n.1471C>G
ENST00000530812.5:n.2488C>G
NM_000383.3:c.738C>G NP_000374.1:p.Ala246=
XM_011529551.1:c.738C>G XP_011527853.1:p.Ala246=
NM_000383.4:c.738C>G MANE Select NP_000374.1:p.Ala246=