Canonical Allele Identifier: CA10051766
Gene: AIRE HGNC NCBI

Linked Data

dbSNP Id: rs747570743

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44290118G>A , CM000683.2:g.44290118G>A GRCh38
NC_000021.8:g.45710001G>A , CM000683.1:g.45710001G>A GRCh37
NC_000021.7:g.44534429G>A NCBI36
NG_009556.1:g.9239G>A , LRG_18:g.9239G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.879+50G>A MANE Select ENSP00000291582.5:n.879+50G>A
ENST00000291582.5:c.879+50G>A ENSP00000291582.5:n.879+50G>A
ENST00000527919.5:n.1612+50G>A
ENST00000530812.5:n.2629+50G>A
NM_000383.3:c.879+50G>A NP_000374.1:n.879+50G>A
XM_011529551.1:c.879+50G>A XP_011527853.1:n.879+50G>A
NM_000383.4:c.879+50G>A MANE Select NP_000374.1:n.879+50G>A