Canonical Allele Identifier: CA342072579
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304669C>G , CM000663.2:g.152304669C>G GRCh38
NC_000001.10:g.152277145C>G , CM000663.1:g.152277145C>G GRCh37
NC_000001.9:g.150543769C>G NCBI36
NG_016190.1:g.25535G>C , LRG_1028:g.25535G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10217G>C MANE Select ENSP00000357789.1:p.Ser3406Thr
ENST00000368799.1:c.10217G>C ENSP00000357789.1:p.Ser3406Thr
NM_002016.1:c.10217G>C , LRG_1028t1:c.10217G>C NP_002007.1:p.Ser3406Thr
XM_011509329.1:c.9109-836G>C XP_011507631.1:n.9109-836G>C
NM_002016.2:c.10217G>C MANE Select NP_002007.1:p.Ser3406Thr