Canonical Allele Identifier: CA410425054
Gene: AIRE HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45712192T>G (hg19) chr21:g.44292309T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44292309T>G , CM000683.2:g.44292309T>G GRCh38
NC_000021.8:g.45712192T>G , CM000683.1:g.45712192T>G GRCh37
NC_000021.7:g.44536620T>G NCBI36
NG_009556.1:g.11430T>G , LRG_18:g.11430T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.1003T>G MANE Select ENSP00000291582.5:p.Trp335Gly
ENST00000291582.5:c.1003T>G ENSP00000291582.5:p.Trp335Gly
ENST00000337909.5:n.464T>G
ENST00000397994.8:n.464T>G
ENST00000527919.5:n.1733T>G
ENST00000530812.5:n.2750T>G
NM_000383.3:c.1003T>G NP_000374.1:p.Trp335Gly
XM_011529551.1:c.1000T>G XP_011527853.1:p.Trp334Gly
NM_000383.4:c.1003T>G MANE Select NP_000374.1:p.Trp335Gly
Search 100 bp 5'
Search 100 bp 3'