Canonical Allele Identifier: CA410426070
Gene: AIRE HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45716272A>C (hg19) chr21:g.44296389A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44296389A>C , CM000683.2:g.44296389A>C GRCh38
NC_000021.8:g.45716272A>C , CM000683.1:g.45716272A>C GRCh37
NC_000021.7:g.44540700A>C NCBI36
NG_009556.1:g.15510A>C , LRG_18:g.15510A>C
NG_034033.1:g.1356A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.1510A>C MANE Select ENSP00000291582.5:p.Thr504Pro
ENST00000291582.5:c.1510A>C ENSP00000291582.5:p.Thr504Pro
ENST00000337909.5:n.971A>C
ENST00000397994.8:n.889A>C
ENST00000527919.5:n.2269A>C
ENST00000530812.5:n.3257A>C
NM_000383.3:c.1510A>C NP_000374.1:p.Thr504Pro
XM_011529551.1:c.1507A>C XP_011527853.1:p.Thr503Pro
NM_000383.4:c.1510A>C MANE Select NP_000374.1:p.Thr504Pro
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