Canonical Allele Identifier: CA1103462
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 265475
dbSNP Id: rs201356558

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304661G>A , CM000663.2:g.152304661G>A GRCh38
NC_000001.10:g.152277137G>A , CM000663.1:g.152277137G>A GRCh37
NC_000001.9:g.150543761G>A NCBI36
NG_016190.1:g.25543C>T , LRG_1028:g.25543C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10225C>T MANE Select ENSP00000357789.1:p.Arg3409Ter
ENST00000368799.1:c.10225C>T ENSP00000357789.1:p.Arg3409Ter
NM_002016.1:c.10225C>T , LRG_1028t1:c.10225C>T NP_002007.1:p.Arg3409Ter
XM_011509329.1:c.9109-828C>T XP_011507631.1:n.9109-828C>T
NM_002016.2:c.10225C>T MANE Select NP_002007.1:p.Arg3409Ter