Canonical Allele Identifier: CA512491000
Gene: AIRE HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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