Canonical Allele Identifier: CA1377326
Gene: IRF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2952881
ClinVar RCV Id: RCV003818015
dbSNP Id: rs781389179

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209795340G>A , CM000663.2:g.209795340G>A GRCh38
NC_000001.10:g.209968685G>A , CM000663.1:g.209968685G>A GRCh37
NC_000001.9:g.208035308G>A NCBI36
NG_007081.2:g.15795C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.458C>T ENSP00000512426.1:p.Ser153Leu
ENST00000696134.1:c.458C>T ENSP00000512427.1:p.Ser153Leu
ENST00000367021.8:c.458C>T MANE Select ENSP00000355988.3:p.Ser153Leu
ENST00000643798.1:c.458C>T ENSP00000496669.1:p.Ser153Leu
ENST00000367021.7:c.458C>T ENSP00000355988.3:p.Ser153Leu
ENST00000456314.1:c.458C>T ENSP00000403855.1:p.Ser153Leu
ENST00000542854.5:c.173C>T ENSP00000440532.1:p.Ser58Leu
NM_001206696.1:c.173C>T NP_001193625.1:p.Ser58Leu
NM_006147.3:c.458C>T NP_006138.1:p.Ser153Leu
NM_006147.4:c.458C>T MANE Select NP_006138.1:p.Ser153Leu
NM_001206696.2:c.173C>T NP_001193625.1:p.Ser58Leu