Canonical Allele Identifier: CA2479951067
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310797C= , CM000663.2:g.152310797C= GRCh38
NC_000001.10:g.152283273C= , CM000663.1:g.152283273C= GRCh37
NC_000001.9:g.150549897C= NCBI36
NG_016190.1:g.19407G= , LRG_1028:g.19407G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4089G= MANE Select ENSP00000357789.1:p.Gln1363=
ENST00000368799.1:c.4089G= ENSP00000357789.1:p.Gln1363=
NM_002016.1:c.4089G= , LRG_1028t1:c.4089G= NP_002007.1:p.Gln1363=
XM_011509329.1:c.4089G= XP_011507631.1:p.Gln1363=
NM_002016.2:c.4089G= MANE Select NP_002007.1:p.Gln1363=