Canonical Allele Identifier: CA10051777
Gene: AIRE HGNC NCBI

Linked Data

dbSNP Id: rs766298373
ExAC: 21:45710670 T / A
gnomAD v2: 21-45710670-T-A
gnomAD v4: 21-44290787-T-A
MyVariant Identifiers: chr21:g.45710670T>A (hg19) chr21:g.44290787T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44290787T>A , CM000683.2:g.44290787T>A GRCh38
NC_000021.8:g.45710670T>A , CM000683.1:g.45710670T>A GRCh37
NC_000021.7:g.44535098T>A NCBI36
NG_009556.1:g.9908T>A , LRG_18:g.9908T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.880-308T>A MANE Select ENSP00000291582.5:n.880-308T>A
ENST00000291582.5:c.880-308T>A ENSP00000291582.5:n.880-308T>A
ENST00000337909.5:n.33T>A
ENST00000397994.8:n.33T>A
ENST00000527919.5:n.1613-311T>A
ENST00000530812.5:n.2630-311T>A
NM_000383.3:c.880-308T>A NP_000374.1:n.880-308T>A
XM_011529551.1:c.880-311T>A XP_011527853.1:n.880-311T>A
NM_000383.4:c.880-308T>A MANE Select NP_000374.1:n.880-308T>A
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