Canonical Allele Identifier: CA1146100439
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312260A= , CM000663.2:g.152312260A= GRCh38
NC_000001.10:g.152284736A= , CM000663.1:g.152284736A= GRCh37
NC_000001.9:g.150551360A= NCBI36
NG_016190.1:g.17944T= , LRG_1028:g.17944T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2626T= MANE Select ENSP00000357789.1:p.Ser876=
ENST00000368799.1:c.2626T= ENSP00000357789.1:p.Ser876=
NM_002016.1:c.2626T= , LRG_1028t1:c.2626T= NP_002007.1:p.Ser876=
XM_011509329.1:c.2626T= XP_011507631.1:p.Ser876=
NM_002016.2:c.2626T= MANE Select NP_002007.1:p.Ser876=