Canonical Allele Identifier: CA2650336322

Gene: IRF6

Linked Data

• gnomAD v4: 1-209795266-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209795266G>T , CM000663.2:g.209795266G>T	GRCh38
NC_000001.10:g.209968611G>T , CM000663.1:g.209968611G>T	GRCh37
NC_000001.9:g.208035234G>T	NCBI36
NG_007081.2:g.15869C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.508+24C>A	ENSP00000512426.1:n.508+24C>A
ENST00000696134.1:c.508+24C>A	ENSP00000512427.1:n.508+24C>A
ENST00000367021.8:c.508+24C>A MANE Select	ENSP00000355988.3:n.508+24C>A
ENST00000643798.1:c.508+24C>A	ENSP00000496669.1:n.508+24C>A
ENST00000367021.7:c.508+24C>A	ENSP00000355988.3:n.508+24C>A
ENST00000456314.1:c.508+24C>A	ENSP00000403855.1:n.508+24C>A
ENST00000542854.5:c.223+24C>A	ENSP00000440532.1:n.223+24C>A
NM_001206696.1:c.223+24C>A	NP_001193625.1:n.223+24C>A
NM_006147.3:c.508+24C>A	NP_006138.1:n.508+24C>A
NM_006147.4:c.508+24C>A MANE Select	NP_006138.1:n.508+24C>A
NM_001206696.2:c.223+24C>A	NP_001193625.1:n.223+24C>A