Canonical Allele Identifier: CA2650336203

Gene: IRF6

Linked Data

• gnomAD v4: 1-209801197-A-ATCC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801197_209801198insTCC , CM000663.2:g.209801197_209801198insTCC	GRCh38
NC_000001.10:g.209974542_209974543insTCC , CM000663.1:g.209974542_209974543insTCC	GRCh37
NC_000001.9:g.208041165_208041166insTCC	NCBI36
NG_007081.2:g.9937_9938insGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.174+42_174+43insGGA	ENSP00000512426.1:n.174+42_174+43insGGA
ENST00000696134.1:c.174+42_174+43insGGA	ENSP00000512427.1:n.174+42_174+43insGGA
ENST00000367021.8:c.174+42_174+43insGGA MANE Select	ENSP00000355988.3:n.174+42_174+43insGGA
ENST00000643798.1:c.174+42_174+43insGGA	ENSP00000496669.1:n.174+42_174+43insGGA
ENST00000367021.7:c.174+42_174+43insGGA	ENSP00000355988.3:n.174+42_174+43insGGA
ENST00000456314.1:c.174+42_174+43insGGA	ENSP00000403855.1:n.174+42_174+43insGGA
ENST00000542854.5:c.-111-4646_-111-4645insGGA	ENSP00000440532.1:n.-111-4646_-111-4645insGGA
NM_001206696.1:c.-111-4646_-111-4645insGGA	NP_001193625.1:n.-111-4646_-111-4645insGGA
NM_006147.3:c.174+42_174+43insGGA	NP_006138.1:n.174+42_174+43insGGA
NM_006147.4:c.174+42_174+43insGGA MANE Select	NP_006138.1:n.174+42_174+43insGGA
NM_001206696.2:c.-111-4646_-111-4645insGGA	NP_001193625.1:n.-111-4646_-111-4645insGGA