Canonical Allele Identifier: CA2479950897
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310998T= , CM000663.2:g.152310998T= GRCh38
NC_000001.10:g.152283474T= , CM000663.1:g.152283474T= GRCh37
NC_000001.9:g.150550098T= NCBI36
NG_016190.1:g.19206A= , LRG_1028:g.19206A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3888A= MANE Select ENSP00000357789.1:p.Gly1296=
ENST00000368799.1:c.3888A= ENSP00000357789.1:p.Gly1296=
NM_002016.1:c.3888A= , LRG_1028t1:c.3888A= NP_002007.1:p.Gly1296=
XM_011509329.1:c.3888A= XP_011507631.1:p.Gly1296=
NM_002016.2:c.3888A= MANE Select NP_002007.1:p.Gly1296=