Canonical Allele Identifier: CA2479951894
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312388G= , CM000663.2:g.152312388G= GRCh38
NC_000001.10:g.152284864G= , CM000663.1:g.152284864G= GRCh37
NC_000001.9:g.150551488G= NCBI36
NG_016190.1:g.17816C= , LRG_1028:g.17816C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2498C= MANE Select ENSP00000357789.1:p.Ala833=
ENST00000368799.1:c.2498C= ENSP00000357789.1:p.Ala833=
NM_002016.1:c.2498C= , LRG_1028t1:c.2498C= NP_002007.1:p.Ala833=
XM_011509329.1:c.2498C= XP_011507631.1:p.Ala833=
NM_002016.2:c.2498C= MANE Select NP_002007.1:p.Ala833=