Canonical Allele Identifier: CA423025761

Gene: IRF6

Linked Data

• MyVariant Identifiers: chr1:g.209961888G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209788543G>A , CM000663.2:g.209788543G>A	GRCh38
NC_000001.10:g.209961888G>A , CM000663.1:g.209961888G>A	GRCh37
NC_000001.9:g.208028511G>A	NCBI36
NG_007081.2:g.22592C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.1281C>T	ENSP00000512426.1:p.Asp427=
ENST00000696134.1:c.*708C>T	ENSP00000512427.1:n.*708C>T
ENST00000367021.8:c.1281C>T MANE Select	ENSP00000355988.3:p.Asp427=
ENST00000643798.1:c.*791C>T	ENSP00000496669.1:n.*791C>T
ENST00000367021.7:c.1281C>T	ENSP00000355988.3:p.Asp427=
ENST00000542854.5:c.996C>T	ENSP00000440532.1:p.Asp332=
NM_001206696.1:c.996C>T	NP_001193625.1:p.Asp332=
NM_006147.3:c.1281C>T	NP_006138.1:p.Asp427=
NM_006147.4:c.1281C>T MANE Select	NP_006138.1:p.Asp427=
NM_001206696.2:c.996C>T	NP_001193625.1:p.Asp332=