Canonical Allele Identifier: CA410424919
Gene: AIRE HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.45711038T>C (hg19) chr21:g.44291155T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44291155T>C , CM000683.2:g.44291155T>C GRCh38
NC_000021.8:g.45711038T>C , CM000683.1:g.45711038T>C GRCh37
NC_000021.7:g.44535466T>C NCBI36
NG_009556.1:g.10276T>C , LRG_18:g.10276T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.940T>C MANE Select ENSP00000291582.5:p.Cys314Arg
ENST00000291582.5:c.940T>C ENSP00000291582.5:p.Cys314Arg
ENST00000337909.5:n.401T>C
ENST00000397994.8:n.401T>C
ENST00000527919.5:n.1670T>C
ENST00000530812.5:n.2687T>C
NM_000383.3:c.940T>C NP_000374.1:p.Cys314Arg
XM_011529551.1:c.937T>C XP_011527853.1:p.Cys313Arg
NM_000383.4:c.940T>C MANE Select NP_000374.1:p.Cys314Arg
Search 100 bp 5'
Search 100 bp 3'