Canonical Allele Identifier: CA2479952267
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313069C= , CM000663.2:g.152313069C= GRCh38
NC_000001.10:g.152285545C= , CM000663.1:g.152285545C= GRCh37
NC_000001.9:g.150552169C= NCBI36
NG_016190.1:g.17135G= , LRG_1028:g.17135G=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.1817G= MANE Select ENSP00000357789.1:p.Gly606=
ENST00000368799.1:c.1817G= ENSP00000357789.1:p.Gly606=
NM_002016.1:c.1817G= , LRG_1028t1:c.1817G= NP_002007.1:p.Gly606=
XM_011509329.1:c.1817G= XP_011507631.1:p.Gly606=
NM_002016.2:c.1817G= MANE Select NP_002007.1:p.Gly606=