Canonical Allele Identifier: CA2479950634
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310016C= , CM000663.2:g.152310016C= GRCh38
NC_000001.10:g.152282492C= , CM000663.1:g.152282492C= GRCh37
NC_000001.9:g.150549116C= NCBI36
NG_016190.1:g.20188G= , LRG_1028:g.20188G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4870G= MANE Select ENSP00000357789.1:p.Glu1624=
ENST00000368799.1:c.4870G= ENSP00000357789.1:p.Glu1624=
NM_002016.1:c.4870G= , LRG_1028t1:c.4870G= NP_002007.1:p.Glu1624=
XM_011509329.1:c.4870G= XP_011507631.1:p.Glu1624=
NM_002016.2:c.4870G= MANE Select NP_002007.1:p.Glu1624=