Canonical Allele Identifier: CA342080887
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311057C>T , CM000663.2:g.152311057C>T GRCh38
NC_000001.10:g.152283533C>T , CM000663.1:g.152283533C>T GRCh37
NC_000001.9:g.150550157C>T NCBI36
NG_016190.1:g.19147G>A , LRG_1028:g.19147G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.3829G>A MANE Select ENSP00000357789.1:p.Glu1277Lys
ENST00000368799.1:c.3829G>A ENSP00000357789.1:p.Glu1277Lys
NM_002016.1:c.3829G>A , LRG_1028t1:c.3829G>A NP_002007.1:p.Glu1277Lys
XM_011509329.1:c.3829G>A XP_011507631.1:p.Glu1277Lys
NM_002016.2:c.3829G>A MANE Select NP_002007.1:p.Glu1277Lys