Canonical Allele Identifier: CA2479950111
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309139G= , CM000663.2:g.152309139G= GRCh38
NC_000001.10:g.152281615G= , CM000663.1:g.152281615G= GRCh37
NC_000001.9:g.150548239G= NCBI36
NG_016190.1:g.21065C= , LRG_1028:g.21065C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5747C= MANE Select ENSP00000357789.1:p.Ser1916=
ENST00000368799.1:c.5747C= ENSP00000357789.1:p.Ser1916=
NM_002016.1:c.5747C= , LRG_1028t1:c.5747C= NP_002007.1:p.Ser1916=
XM_011509329.1:c.5747C= XP_011507631.1:p.Ser1916=
NM_002016.2:c.5747C= MANE Select NP_002007.1:p.Ser1916=