Canonical Allele Identifier: CA1145824000
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309086A= , CM000663.2:g.152309086A= GRCh38
NC_000001.10:g.152281562A= , CM000663.1:g.152281562A= GRCh37
NC_000001.9:g.150548186A= NCBI36
NG_016190.1:g.21118T= , LRG_1028:g.21118T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5800T= MANE Select ENSP00000357789.1:p.Trp1934=
ENST00000368799.1:c.5800T= ENSP00000357789.1:p.Trp1934=
NM_002016.1:c.5800T= , LRG_1028t1:c.5800T= NP_002007.1:p.Trp1934=
XM_011509329.1:c.5800T= XP_011507631.1:p.Trp1934=
NM_002016.2:c.5800T= MANE Select NP_002007.1:p.Trp1934=