Canonical Allele Identifier: CA749685161

Gene: AIRE

Linked Data

• dbSNP Id: rs1185499766
• MyVariant Identifiers: chr21:g.45716236G>T (hg19) ; chr21:g.44296353G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44296353G>T , CM000683.2:g.44296353G>T	GRCh38
NC_000021.8:g.45716236G>T , CM000683.1:g.45716236G>T	GRCh37
NC_000021.7:g.44540664G>T	NCBI36
NG_009556.1:g.15474G>T , LRG_18:g.15474G>T
NG_034033.1:g.1320G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000291582.6:c.1504-30G>T MANE Select	ENSP00000291582.5:n.1504-30G>T
ENST00000291582.5:c.1504-30G>T	ENSP00000291582.5:n.1504-30G>T
ENST00000337909.5:n.965-30G>T
ENST00000397994.8:n.883-30G>T
ENST00000527919.5:n.2263-30G>T
ENST00000530812.5:n.3251-30G>T
NM_000383.3:c.1504-30G>T	NP_000374.1:n.1504-30G>T
XM_011529551.1:c.1501-30G>T	XP_011527853.1:n.1501-30G>T
NM_000383.4:c.1504-30G>T MANE Select	NP_000374.1:n.1504-30G>T