Canonical Allele Identifier: CA2479947618
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304751T= , CM000663.2:g.152304751T= GRCh38
NC_000001.10:g.152277227T= , CM000663.1:g.152277227T= GRCh37
NC_000001.9:g.150543851T= NCBI36
NG_016190.1:g.25453A= , LRG_1028:g.25453A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10135A= MANE Select ENSP00000357789.1:p.Arg3379=
ENST00000368799.1:c.10135A= ENSP00000357789.1:p.Arg3379=
NM_002016.1:c.10135A= , LRG_1028t1:c.10135A= NP_002007.1:p.Arg3379=
XM_011509329.1:c.9109-918A= XP_011507631.1:n.9109-918A=
NM_002016.2:c.10135A= MANE Select NP_002007.1:p.Arg3379=