Canonical Allele Identifier: CA344585788

Gene: IRF6

Linked Data

• MyVariant Identifiers: chr1:g.209974670T>G (hg19) ; chr1:g.209801325T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801325T>G , CM000663.2:g.209801325T>G	GRCh38
NC_000001.10:g.209974670T>G , CM000663.1:g.209974670T>G	GRCh37
NC_000001.9:g.208041293T>G	NCBI36
NG_007081.2:g.9810A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696133.1:c.89A>C	ENSP00000512426.1:p.His30Pro
ENST00000696134.1:c.89A>C	ENSP00000512427.1:p.His30Pro
ENST00000367021.8:c.89A>C MANE Select	ENSP00000355988.3:p.His30Pro
ENST00000643798.1:c.89A>C	ENSP00000496669.1:p.His30Pro
ENST00000367021.7:c.89A>C	ENSP00000355988.3:p.His30Pro
ENST00000456314.1:c.89A>C	ENSP00000403855.1:p.His30Pro
ENST00000542854.5:c.-112+4622A>C	ENSP00000440532.1:n.-112+4622A>C
NM_001206696.1:c.-112+4622A>C	NP_001193625.1:n.-112+4622A>C
NM_006147.3:c.89A>C	NP_006138.1:p.His30Pro
NM_006147.4:c.89A>C MANE Select	NP_006138.1:p.His30Pro
NM_001206696.2:c.-112+4622A>C	NP_001193625.1:n.-112+4622A>C