Canonical Allele Identifier: CA1107840
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3040440
ClinVar RCV Id: RCV003926821
dbSNP Id: rs146115338
COSMIC: COSM118761

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313911C>T , CM000663.2:g.152313911C>T GRCh38
NC_000001.10:g.152286387C>T , CM000663.1:g.152286387C>T GRCh37
NC_000001.9:g.150553011C>T NCBI36
NG_016190.1:g.16293G>A , LRG_1028:g.16293G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.975G>A MANE Select ENSP00000357789.1:p.Ala325=
ENST00000368799.1:c.975G>A ENSP00000357789.1:p.Ala325=
NM_002016.1:c.975G>A , LRG_1028t1:c.975G>A NP_002007.1:p.Ala325=
NR_103778.1:n.453C>T
XM_011509329.1:c.975G>A XP_011507631.1:p.Ala325=
NM_002016.2:c.975G>A MANE Select NP_002007.1:p.Ala325=