Canonical Allele Identifier: CA1139986948
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311335G= , CM000663.2:g.152311335G= GRCh38
NC_000001.10:g.152283811G= , CM000663.1:g.152283811G= GRCh37
NC_000001.9:g.150550435G= NCBI36
NG_016190.1:g.18869C= , LRG_1028:g.18869C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3551C= MANE Select ENSP00000357789.1:p.Ser1184=
ENST00000368799.1:c.3551C= ENSP00000357789.1:p.Ser1184=
NM_002016.1:c.3551C= , LRG_1028t1:c.3551C= NP_002007.1:p.Ser1184=
XM_011509329.1:c.3551C= XP_011507631.1:p.Ser1184=
NM_002016.2:c.3551C= MANE Select NP_002007.1:p.Ser1184=