Canonical Allele Identifier: CA1139656523
Gene: IRF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 872903
ClinVar RCV Id: RCV001093600
dbSNP Id: rs2077939646

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801229_209801278del , CM000663.2:g.209801229_209801278del GRCh38
NC_000001.10:g.209974574_209974623del , CM000663.1:g.209974574_209974623del GRCh37
NC_000001.9:g.208041197_208041246del NCBI36
NG_007081.2:g.9858_9907del

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.137_174+12del
ENST00000696134.1:c.137_174+12del
ENST00000367021.8:c.137_174+12del
ENST00000643798.1:c.137_174+12del
ENST00000367021.7:c.137_174+12del
ENST00000456314.1:c.137_174+12del
ENST00000542854.5:c.-112+4670_-111-4676del ENSP00000440532.1:n.-112+4670_-111-4676de...
NM_001206696.1:c.-112+4670_-111-4676del NP_001193625.1:n.-112+4670_-111-4676del
NM_006147.3:c.137_174+12del
NM_006147.4:c.137_174+12del
NM_001206696.2:c.-112+4670_-111-4676del NP_001193625.1:n.-112+4670_-111-4676del