Canonical Allele Identifier: CA730861729

Gene: IRF6

Linked Data

• MyVariant Identifiers: chr1:g.209974549_209974550insAT (hg19) ; chr1:g.209801204_209801205insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801204_209801205insAT , CM000663.2:g.209801204_209801205insAT	GRCh38
NC_000001.10:g.209974549_209974550insAT , CM000663.1:g.209974549_209974550insAT	GRCh37
NC_000001.9:g.208041172_208041173insAT	NCBI36
NG_007081.2:g.9930_9931insAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000696133.1:c.174+35_174+36insAT	ENSP00000512426.1:n.174+35_174+36insAT
ENST00000696134.1:c.174+35_174+36insAT	ENSP00000512427.1:n.174+35_174+36insAT
ENST00000367021.8:c.174+35_174+36insAT MANE Select	ENSP00000355988.3:n.174+35_174+36insAT
ENST00000643798.1:c.174+35_174+36insAT	ENSP00000496669.1:n.174+35_174+36insAT
ENST00000367021.7:c.174+35_174+36insAT	ENSP00000355988.3:n.174+35_174+36insAT
ENST00000456314.1:c.174+35_174+36insAT	ENSP00000403855.1:n.174+35_174+36insAT
ENST00000542854.5:c.-111-4653_-111-4652insAT	ENSP00000440532.1:n.-111-4653_-111-4652insAT
NM_001206696.1:c.-111-4653_-111-4652insAT	NP_001193625.1:n.-111-4653_-111-4652insAT
NM_006147.3:c.174+35_174+36insAT	NP_006138.1:n.174+35_174+36insAT
NM_006147.4:c.174+35_174+36insAT MANE Select	NP_006138.1:n.174+35_174+36insAT
NM_001206696.2:c.-111-4653_-111-4652insAT	NP_001193625.1:n.-111-4653_-111-4652insAT