Canonical Allele Identifier: CA1141681427
Gene: FLG HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.3829G= MANE Select ENSP00000357789.1:p.Glu1277=
ENST00000368799.1:c.3829G= ENSP00000357789.1:p.Glu1277=
NM_002016.1:c.3829G= , LRG_1028t1:c.3829G= NP_002007.1:p.Glu1277=
XM_011509329.1:c.3829G= XP_011507631.1:p.Glu1277=
NM_002016.2:c.3829G= MANE Select NP_002007.1:p.Glu1277=