Canonical Allele Identifier: CA410423213

Gene: AIRE

Linked Data

• gnomAD v4: 21-44286566-C-T
• MyVariant Identifiers: chr21:g.45706449C>T (hg19) ; chr21:g.44286566C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44286566C>T , CM000683.2:g.44286566C>T	GRCh38
NC_000021.8:g.45706449C>T , CM000683.1:g.45706449C>T	GRCh37
NC_000021.7:g.44530877C>T	NCBI36
NG_009556.1:g.5687C>T , LRG_18:g.5687C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000291582.6:c.142C>T MANE Select	ENSP00000291582.5:p.His48Tyr
ENST00000291582.5:c.142C>T	ENSP00000291582.5:p.His48Tyr
ENST00000527919.5:n.303C>T
ENST00000530812.5:n.311C>T
NM_000383.3:c.142C>T	NP_000374.1:p.His48Tyr
XM_011529551.1:c.142C>T	XP_011527853.1:p.His48Tyr
NM_000383.4:c.142C>T MANE Select	NP_000374.1:p.His48Tyr