Canonical Allele Identifier: CA2650336349

Gene: IRF6

Linked Data

• gnomAD v4: 1-209795460-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209795460G>T , CM000663.2:g.209795460G>T	GRCh38
NC_000001.10:g.209968805G>T , CM000663.1:g.209968805G>T	GRCh37
NC_000001.9:g.208035428G>T	NCBI36
NG_007081.2:g.15675C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.380-42C>A	ENSP00000512426.1:n.380-42C>A
ENST00000696134.1:c.380-42C>A	ENSP00000512427.1:n.380-42C>A
ENST00000367021.8:c.380-42C>A MANE Select	ENSP00000355988.3:n.380-42C>A
ENST00000643798.1:c.380-42C>A	ENSP00000496669.1:n.380-42C>A
ENST00000367021.7:c.380-42C>A	ENSP00000355988.3:n.380-42C>A
ENST00000456314.1:c.380-42C>A	ENSP00000403855.1:n.380-42C>A
ENST00000542854.5:c.95-42C>A	ENSP00000440532.1:n.95-42C>A
NM_001206696.1:c.95-42C>A	NP_001193625.1:n.95-42C>A
NM_006147.3:c.380-42C>A	NP_006138.1:n.380-42C>A
NM_006147.4:c.380-42C>A MANE Select	NP_006138.1:n.380-42C>A
NM_001206696.2:c.95-42C>A	NP_001193625.1:n.95-42C>A