Canonical Allele Identifier: CA342089730
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs745516434

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312459C>A , CM000663.2:g.152312459C>A GRCh38
NC_000001.10:g.152284935C>A , CM000663.1:g.152284935C>A GRCh37
NC_000001.9:g.150551559C>A NCBI36
NG_016190.1:g.17745G>T , LRG_1028:g.17745G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2427G>T MANE Select ENSP00000357789.1:p.Trp809Cys
ENST00000368799.1:c.2427G>T ENSP00000357789.1:p.Trp809Cys
NM_002016.1:c.2427G>T , LRG_1028t1:c.2427G>T NP_002007.1:p.Trp809Cys
XM_011509329.1:c.2427G>T XP_011507631.1:p.Trp809Cys
NM_002016.2:c.2427G>T MANE Select NP_002007.1:p.Trp809Cys