Canonical Allele Identifier: CA1144371899
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313901A= , CM000663.2:g.152313901A= GRCh38
NC_000001.10:g.152286377A= , CM000663.1:g.152286377A= GRCh37
NC_000001.9:g.150553001A= NCBI36
NG_016190.1:g.16303T= , LRG_1028:g.16303T=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.985T= MANE Select ENSP00000357789.1:p.Ser329=
ENST00000368799.1:c.985T= ENSP00000357789.1:p.Ser329=
NM_002016.1:c.985T= , LRG_1028t1:c.985T= NP_002007.1:p.Ser329=
NR_103778.1:n.443A=
XM_011509329.1:c.985T= XP_011507631.1:p.Ser329=
NM_002016.2:c.985T= MANE Select NP_002007.1:p.Ser329=