Canonical Allele Identifier: CA344572602

Gene: IRF6

Linked Data

• MyVariant Identifiers: chr1:g.209961795C>G (hg19) ; chr1:g.209788450C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209788450C>G , CM000663.2:g.209788450C>G	GRCh38
NC_000001.10:g.209961795C>G , CM000663.1:g.209961795C>G	GRCh37
NC_000001.9:g.208028418C>G	NCBI36
NG_007081.2:g.22685G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696133.1:c.1374G>C	ENSP00000512426.1:p.Met458Ile
ENST00000696134.1:c.*801G>C	ENSP00000512427.1:n.*801G>C
ENST00000367021.8:c.1374G>C MANE Select	ENSP00000355988.3:p.Met458Ile
ENST00000643798.1:c.*884G>C	ENSP00000496669.1:n.*884G>C
ENST00000367021.7:c.1374G>C	ENSP00000355988.3:p.Met458Ile
ENST00000542854.5:c.1089G>C	ENSP00000440532.1:p.Met363Ile
NM_001206696.1:c.1089G>C	NP_001193625.1:p.Met363Ile
NM_006147.3:c.1374G>C	NP_006138.1:p.Met458Ile
NM_006147.4:c.1374G>C MANE Select	NP_006138.1:p.Met458Ile
NM_001206696.2:c.1089G>C	NP_001193625.1:p.Met363Ile