Canonical Allele Identifier: CA1103636
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs750013989

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305005G>A , CM000663.2:g.152305005G>A GRCh38
NC_000001.10:g.152277481G>A , CM000663.1:g.152277481G>A GRCh37
NC_000001.9:g.150544105G>A NCBI36
NG_016190.1:g.25199C>T , LRG_1028:g.25199C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9881C>T MANE Select ENSP00000357789.1:p.Ala3294Val
ENST00000368799.1:c.9881C>T ENSP00000357789.1:p.Ala3294Val
NM_002016.1:c.9881C>T , LRG_1028t1:c.9881C>T NP_002007.1:p.Ala3294Val
XM_011509329.1:c.9108+773C>T XP_011507631.1:n.9108+773C>T
NM_002016.2:c.9881C>T MANE Select NP_002007.1:p.Ala3294Val