Canonical Allele Identifier: CA1103392
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs776849211

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304533C>A , CM000663.2:g.152304533C>A GRCh38
NC_000001.10:g.152277009C>A , CM000663.1:g.152277009C>A GRCh37
NC_000001.9:g.150543633C>A NCBI36
NG_016190.1:g.25671G>T , LRG_1028:g.25671G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10353G>T MANE Select ENSP00000357789.1:p.Glu3451Asp
ENST00000368799.1:c.10353G>T ENSP00000357789.1:p.Glu3451Asp
NM_002016.1:c.10353G>T , LRG_1028t1:c.10353G>T NP_002007.1:p.Glu3451Asp
XM_011509329.1:c.9109-700G>T XP_011507631.1:n.9109-700G>T
NM_002016.2:c.10353G>T MANE Select NP_002007.1:p.Glu3451Asp