Canonical Allele Identifier: CA342103900
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs529065322

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.985T>A MANE Select ENSP00000357789.1:p.Ser329Thr
ENST00000368799.1:c.985T>A ENSP00000357789.1:p.Ser329Thr
NM_002016.1:c.985T>A , LRG_1028t1:c.985T>A NP_002007.1:p.Ser329Thr
NR_103778.1:n.443A>T
XM_011509329.1:c.985T>A XP_011507631.1:p.Ser329Thr
NM_002016.2:c.985T>A MANE Select NP_002007.1:p.Ser329Thr