Canonical Allele Identifier: CA410426058
Gene: AIRE HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45716267A>C (hg19) chr21:g.44296384A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44296384A>C , CM000683.2:g.44296384A>C GRCh38
NC_000021.8:g.45716267A>C , CM000683.1:g.45716267A>C GRCh37
NC_000021.7:g.44540695A>C NCBI36
NG_009556.1:g.15505A>C , LRG_18:g.15505A>C
NG_034033.1:g.1351A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.1505A>C MANE Select ENSP00000291582.5:p.Asp502Ala
ENST00000291582.5:c.1505A>C ENSP00000291582.5:p.Asp502Ala
ENST00000337909.5:n.966A>C
ENST00000397994.8:n.884A>C
ENST00000527919.5:n.2264A>C
ENST00000530812.5:n.3252A>C
NM_000383.3:c.1505A>C NP_000374.1:p.Asp502Ala
XM_011529551.1:c.1502A>C XP_011527853.1:p.Asp501Ala
NM_000383.4:c.1505A>C MANE Select NP_000374.1:p.Asp502Ala
Search 100 bp 5'
Search 100 bp 3'