Canonical Allele Identifier: CA2479951366
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311435C= , CM000663.2:g.152311435C= GRCh38
NC_000001.10:g.152283911C= , CM000663.1:g.152283911C= GRCh37
NC_000001.9:g.150550535C= NCBI36
NG_016190.1:g.18769G= , LRG_1028:g.18769G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3451G= MANE Select ENSP00000357789.1:p.Asp1151=
ENST00000368799.1:c.3451G= ENSP00000357789.1:p.Asp1151=
NM_002016.1:c.3451G= , LRG_1028t1:c.3451G= NP_002007.1:p.Asp1151=
XM_011509329.1:c.3451G= XP_011507631.1:p.Asp1151=
NM_002016.2:c.3451G= MANE Select NP_002007.1:p.Asp1151=