Canonical Allele Identifier: CA30568291
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1019832328

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313908C>T , CM000663.2:g.152313908C>T GRCh38
NC_000001.10:g.152286384C>T , CM000663.1:g.152286384C>T GRCh37
NC_000001.9:g.150553008C>T NCBI36
NG_016190.1:g.16296G>A , LRG_1028:g.16296G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.978G>A MANE Select ENSP00000357789.1:p.Trp326Ter
ENST00000368799.1:c.978G>A ENSP00000357789.1:p.Trp326Ter
NM_002016.1:c.978G>A , LRG_1028t1:c.978G>A NP_002007.1:p.Trp326Ter
NR_103778.1:n.450C>T
XM_011509329.1:c.978G>A XP_011507631.1:p.Trp326Ter
NM_002016.2:c.978G>A MANE Select NP_002007.1:p.Trp326Ter