Canonical Allele Identifier: CA1103461
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs201356558

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10225C>G MANE Select ENSP00000357789.1:p.Arg3409Gly
ENST00000368799.1:c.10225C>G ENSP00000357789.1:p.Arg3409Gly
NM_002016.1:c.10225C>G , LRG_1028t1:c.10225C>G NP_002007.1:p.Arg3409Gly
XM_011509329.1:c.9109-828C>G XP_011507631.1:n.9109-828C>G
NM_002016.2:c.10225C>G MANE Select NP_002007.1:p.Arg3409Gly