Canonical Allele Identifier: CA2479947787
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305036C= , CM000663.2:g.152305036C= GRCh38
NC_000001.10:g.152277512C= , CM000663.1:g.152277512C= GRCh37
NC_000001.9:g.150544136C= NCBI36
NG_016190.1:g.25168G= , LRG_1028:g.25168G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9850G= MANE Select ENSP00000357789.1:p.Gly3284=
ENST00000368799.1:c.9850G= ENSP00000357789.1:p.Gly3284=
NM_002016.1:c.9850G= , LRG_1028t1:c.9850G= NP_002007.1:p.Gly3284=
XM_011509329.1:c.9108+742G= XP_011507631.1:n.9108+742G=
NM_002016.2:c.9850G= MANE Select NP_002007.1:p.Gly3284=