Canonical Allele Identifier: CA2484369532

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801199_209801205delinsAAAAAAT , CM000663.2:g.209801199_209801205delinsAAAAAAT	GRCh38
NC_000001.10:g.209974544_209974550delinsAAAAAAT , CM000663.1:g.209974544_209974550delinsAAAAAAT	GRCh37
NC_000001.9:g.208041167_208041173delinsAAAAAAT	NCBI36
NG_007081.2:g.9930_9936delinsATTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.174+35_174+41delinsATTTTTT	ENSP00000512426.1:n.174+35_174+41delinsATTTTTT
ENST00000696134.1:c.174+35_174+41delinsATTTTTT	ENSP00000512427.1:n.174+35_174+41delinsATTTTTT
ENST00000367021.8:c.174+35_174+41delinsATTTTTT MANE Select	ENSP00000355988.3:n.174+35_174+41delinsATTTTTT
ENST00000643798.1:c.174+35_174+41delinsATTTTTT	ENSP00000496669.1:n.174+35_174+41delinsATTTTTT
ENST00000367021.7:c.174+35_174+41delinsATTTTTT	ENSP00000355988.3:n.174+35_174+41delinsATTTTTT
ENST00000456314.1:c.174+35_174+41delinsATTTTTT	ENSP00000403855.1:n.174+35_174+41delinsATTTTTT
ENST00000542854.5:c.-111-4653_-111-4647delinsATTTTTT	ENSP00000440532.1:n.-111-4653_-111-4647delinsATTTTTT
NM_001206696.1:c.-111-4653_-111-4647delinsATTTTTT	NP_001193625.1:n.-111-4653_-111-4647delinsATTTTTT
NM_006147.3:c.174+35_174+41delinsATTTTTT	NP_006138.1:n.174+35_174+41delinsATTTTTT
NM_006147.4:c.174+35_174+41delinsATTTTTT MANE Select	NP_006138.1:n.174+35_174+41delinsATTTTTT
NM_001206696.2:c.-111-4653_-111-4647delinsATTTTTT	NP_001193625.1:n.-111-4653_-111-4647delinsATTTTTT