Canonical Allele Identifier: CA512491013
Gene: AIRE HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45709658A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44289775A>G , CM000683.2:g.44289775A>G GRCh38
NC_000021.8:g.45709658A>G , CM000683.1:g.45709658A>G GRCh37
NC_000021.7:g.44534086A>G NCBI36
NG_009556.1:g.8896A>G , LRG_18:g.8896A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.771A>G MANE Select ENSP00000291582.5:p.Arg257=
ENST00000291582.5:c.771A>G ENSP00000291582.5:p.Arg257=
ENST00000527919.5:n.1504A>G
ENST00000530812.5:n.2521A>G
NM_000383.3:c.771A>G NP_000374.1:p.Arg257=
XM_011529551.1:c.771A>G XP_011527853.1:p.Arg257=
NM_000383.4:c.771A>G MANE Select NP_000374.1:p.Arg257=