Canonical Allele Identifier: CA2479950108
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309135A= , CM000663.2:g.152309135A= GRCh38
NC_000001.10:g.152281611A= , CM000663.1:g.152281611A= GRCh37
NC_000001.9:g.150548235A= NCBI36
NG_016190.1:g.21069T= , LRG_1028:g.21069T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5751T= MANE Select ENSP00000357789.1:p.Ser1917=
ENST00000368799.1:c.5751T= ENSP00000357789.1:p.Ser1917=
NM_002016.1:c.5751T= , LRG_1028t1:c.5751T= NP_002007.1:p.Ser1917=
XM_011509329.1:c.5751T= XP_011507631.1:p.Ser1917=
NM_002016.2:c.5751T= MANE Select NP_002007.1:p.Ser1917=