Canonical Allele Identifier: CA2484364123
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209786349A= , CM000663.2:g.209786349A= GRCh38
NC_000001.10:g.209959694A= , CM000663.1:g.209959694A= GRCh37
NC_000001.9:g.208026317A= NCBI36
NG_007081.2:g.24786T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1400+2075T= ENSP00000512426.1:n.1400+2075T=
ENST00000696134.1:c.*2902T= ENSP00000512427.1:n.*2902T=
ENST00000367021.8:c.*2071T= MANE Select ENSP00000355988.3:n.*2071T=
ENST00000367021.7:c.*2071T= ENSP00000355988.3:n.*2071T=
ENST00000542854.5:c.*2071T= ENSP00000440532.1:n.*2071T=
NM_001206696.1:c.*2071T= NP_001193625.1:n.*2071T=
NM_006147.3:c.*2071T= NP_006138.1:n.*2071T=
NM_006147.4:c.*2071T= MANE Select NP_006138.1:n.*2071T=
NM_001206696.2:c.*2071T= NP_001193625.1:n.*2071T=