Canonical Allele Identifier: CA512490997
Gene: AIRE HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45709649T>A (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.762T>A MANE Select ENSP00000291582.5:p.Pro254=
ENST00000291582.5:c.762T>A ENSP00000291582.5:p.Pro254=
ENST00000527919.5:n.1495T>A
ENST00000530812.5:n.2512T>A
NM_000383.3:c.762T>A NP_000374.1:p.Pro254=
XM_011529551.1:c.762T>A XP_011527853.1:p.Pro254=
NM_000383.4:c.762T>A MANE Select NP_000374.1:p.Pro254=
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Search 100 bp 3'