Canonical Allele Identifier: CA2484364029
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209786124T= , CM000663.2:g.209786124T= GRCh38
NC_000001.10:g.209959469T= , CM000663.1:g.209959469T= GRCh37
NC_000001.9:g.208026092T= NCBI36
NG_007081.2:g.25011A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.1400+2300A= ENSP00000512426.1:n.1400+2300A=
ENST00000696134.1:c.*3127A= ENSP00000512427.1:n.*3127A=
ENST00000367021.8:c.*2296A= MANE Select ENSP00000355988.3:n.*2296A=
ENST00000367021.7:c.*2296A= ENSP00000355988.3:n.*2296A=
ENST00000542854.5:c.*2296A= ENSP00000440532.1:n.*2296A=
NM_001206696.1:c.*2296A= NP_001193625.1:n.*2296A=
NM_006147.3:c.*2296A= NP_006138.1:n.*2296A=
NM_006147.4:c.*2296A= MANE Select NP_006138.1:n.*2296A=
NM_001206696.2:c.*2296A= NP_001193625.1:n.*2296A=