Canonical Allele Identifier: CA2479951100
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310855G= , CM000663.2:g.152310855G= GRCh38
NC_000001.10:g.152283331G= , CM000663.1:g.152283331G= GRCh37
NC_000001.9:g.150549955G= NCBI36
NG_016190.1:g.19349C= , LRG_1028:g.19349C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4031C= MANE Select ENSP00000357789.1:p.Ser1344=
ENST00000368799.1:c.4031C= ENSP00000357789.1:p.Ser1344=
NM_002016.1:c.4031C= , LRG_1028t1:c.4031C= NP_002007.1:p.Ser1344=
XM_011509329.1:c.4031C= XP_011507631.1:p.Ser1344=
NM_002016.2:c.4031C= MANE Select NP_002007.1:p.Ser1344=