Canonical Allele Identifier: CA1103491
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs769473061

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304704T>A , CM000663.2:g.152304704T>A GRCh38
NC_000001.10:g.152277180T>A , CM000663.1:g.152277180T>A GRCh37
NC_000001.9:g.150543804T>A NCBI36
NG_016190.1:g.25500A>T , LRG_1028:g.25500A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10182A>T MANE Select ENSP00000357789.1:p.Glu3394Asp
ENST00000368799.1:c.10182A>T ENSP00000357789.1:p.Glu3394Asp
NM_002016.1:c.10182A>T , LRG_1028t1:c.10182A>T NP_002007.1:p.Glu3394Asp
XM_011509329.1:c.9109-871A>T XP_011507631.1:n.9109-871A>T
NM_002016.2:c.10182A>T MANE Select NP_002007.1:p.Glu3394Asp