Canonical Allele Identifier: CA2479949737
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308634A= , CM000663.2:g.152308634A= GRCh38
NC_000001.10:g.152281110A= , CM000663.1:g.152281110A= GRCh37
NC_000001.9:g.150547734A= NCBI36
NG_016190.1:g.21570T= , LRG_1028:g.21570T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6252T= MANE Select ENSP00000357789.1:p.Ser2084=
ENST00000368799.1:c.6252T= ENSP00000357789.1:p.Ser2084=
NM_002016.1:c.6252T= , LRG_1028t1:c.6252T= NP_002007.1:p.Ser2084=
XM_011509329.1:c.6252T= XP_011507631.1:p.Ser2084=
NM_002016.2:c.6252T= MANE Select NP_002007.1:p.Ser2084=