Canonical Allele Identifier: CA2479952706
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313898T= , CM000663.2:g.152313898T= GRCh38
NC_000001.10:g.152286374T= , CM000663.1:g.152286374T= GRCh37
NC_000001.9:g.150552998T= NCBI36
NG_016190.1:g.16306A= , LRG_1028:g.16306A=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.988A= MANE Select ENSP00000357789.1:p.Arg330=
ENST00000368799.1:c.988A= ENSP00000357789.1:p.Arg330=
NM_002016.1:c.988A= , LRG_1028t1:c.988A= NP_002007.1:p.Arg330=
NR_103778.1:n.440T=
XM_011509329.1:c.988A= XP_011507631.1:p.Arg330=
NM_002016.2:c.988A= MANE Select NP_002007.1:p.Arg330=