Canonical Allele Identifier: CA2479949882
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308760A= , CM000663.2:g.152308760A= GRCh38
NC_000001.10:g.152281236A= , CM000663.1:g.152281236A= GRCh37
NC_000001.9:g.150547860A= NCBI36
NG_016190.1:g.21444T= , LRG_1028:g.21444T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6126T= MANE Select ENSP00000357789.1:p.Ser2042=
ENST00000368799.1:c.6126T= ENSP00000357789.1:p.Ser2042=
NM_002016.1:c.6126T= , LRG_1028t1:c.6126T= NP_002007.1:p.Ser2042=
XM_011509329.1:c.6126T= XP_011507631.1:p.Ser2042=
NM_002016.2:c.6126T= MANE Select NP_002007.1:p.Ser2042=