Canonical Allele Identifier: CA410424940
Gene: AIRE HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45711050T>A (hg19) chr21:g.44291167T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44291167T>A , CM000683.2:g.44291167T>A GRCh38
NC_000021.8:g.45711050T>A , CM000683.1:g.45711050T>A GRCh37
NC_000021.7:g.44535478T>A NCBI36
NG_009556.1:g.10288T>A , LRG_18:g.10288T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.952T>A MANE Select ENSP00000291582.5:p.Phe318Ile
ENST00000291582.5:c.952T>A ENSP00000291582.5:p.Phe318Ile
ENST00000337909.5:n.413T>A
ENST00000397994.8:n.413T>A
ENST00000527919.5:n.1682T>A
ENST00000530812.5:n.2699T>A
NM_000383.3:c.952T>A NP_000374.1:p.Phe318Ile
XM_011529551.1:c.949T>A XP_011527853.1:p.Phe317Ile
NM_000383.4:c.952T>A MANE Select NP_000374.1:p.Phe318Ile
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