Canonical Allele Identifier: CA512490998

Gene: AIRE

Linked Data

• MyVariant Identifiers: chr21:g.45709649T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44289766T>C , CM000683.2:g.44289766T>C	GRCh38
NC_000021.8:g.45709649T>C , CM000683.1:g.45709649T>C	GRCh37
NC_000021.7:g.44534077T>C	NCBI36
NG_009556.1:g.8887T>C , LRG_18:g.8887T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291582.6:c.762T>C MANE Select	ENSP00000291582.5:p.Pro254=
ENST00000291582.5:c.762T>C	ENSP00000291582.5:p.Pro254=
ENST00000527919.5:n.1495T>C
ENST00000530812.5:n.2512T>C
NM_000383.3:c.762T>C	NP_000374.1:p.Pro254=
XM_011529551.1:c.762T>C	XP_011527853.1:p.Pro254=
NM_000383.4:c.762T>C MANE Select	NP_000374.1:p.Pro254=