Canonical Allele Identifier: CA2484369563
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801282G= , CM000663.2:g.209801282G= GRCh38
NC_000001.10:g.209974627G= , CM000663.1:g.209974627G= GRCh37
NC_000001.9:g.208041250G= NCBI36
NG_007081.2:g.9853C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.132C= ENSP00000512426.1:p.Thr44=
ENST00000696134.1:c.132C= ENSP00000512427.1:p.Thr44=
ENST00000367021.8:c.132C= MANE Select ENSP00000355988.3:p.Thr44=
ENST00000643798.1:c.132C= ENSP00000496669.1:p.Thr44=
ENST00000367021.7:c.132C= ENSP00000355988.3:p.Thr44=
ENST00000456314.1:c.132C= ENSP00000403855.1:p.Thr44=
ENST00000542854.5:c.-112+4665C= ENSP00000440532.1:n.-112+4665C=
NM_001206696.1:c.-112+4665C= NP_001193625.1:n.-112+4665C=
NM_006147.3:c.132C= NP_006138.1:p.Thr44=
NM_006147.4:c.132C= MANE Select NP_006138.1:p.Thr44=
NM_001206696.2:c.-112+4665C= NP_001193625.1:n.-112+4665C=