Canonical Allele Identifier: CA512490695
Gene: AIRE HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45708257A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44288374A>C , CM000683.2:g.44288374A>C GRCh38
NC_000021.8:g.45708257A>C , CM000683.1:g.45708257A>C GRCh37
NC_000021.7:g.44532685A>C NCBI36
NG_009556.1:g.7495A>C , LRG_18:g.7495A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.568A>C MANE Select ENSP00000291582.5:p.Arg190=
ENST00000291582.5:c.568A>C ENSP00000291582.5:p.Arg190=
ENST00000527919.5:n.1112A>C
ENST00000530812.5:n.1120A>C
NM_000383.3:c.568A>C NP_000374.1:p.Arg190=
XM_011529551.1:c.568A>C XP_011527853.1:p.Arg190=
NM_000383.4:c.568A>C MANE Select NP_000374.1:p.Arg190=