Canonical Allele Identifier: CA2391570642
Gene: AIRE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44296486C= , CM000683.2:g.44296486C= GRCh38
NC_000021.8:g.45716369C= , CM000683.1:g.45716369C= GRCh37
NC_000021.7:g.44540797C= NCBI36
NG_009556.1:g.15607C= , LRG_18:g.15607C=
NG_034033.1:g.1453C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.1566+41C= MANE Select ENSP00000291582.5:n.1566+41C=
ENST00000291582.5:c.1566+41C= ENSP00000291582.5:n.1566+41C=
ENST00000337909.5:n.1027+41C=
ENST00000397994.8:n.945+41C=
ENST00000527919.5:n.2325+41C=
ENST00000530812.5:n.3313+41C=
NM_000383.3:c.1566+41C= NP_000374.1:n.1566+41C=
XM_011529551.1:c.1563+41C= XP_011527853.1:n.1563+41C=
NM_000383.4:c.1566+41C= MANE Select NP_000374.1:n.1566+41C=