Canonical Allele Identifier: CA2479947769
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305004T= , CM000663.2:g.152305004T= GRCh38
NC_000001.10:g.152277480T= , CM000663.1:g.152277480T= GRCh37
NC_000001.9:g.150544104T= NCBI36
NG_016190.1:g.25200A= , LRG_1028:g.25200A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9882A= MANE Select ENSP00000357789.1:p.Ala3294=
ENST00000368799.1:c.9882A= ENSP00000357789.1:p.Ala3294=
NM_002016.1:c.9882A= , LRG_1028t1:c.9882A= NP_002007.1:p.Ala3294=
XM_011509329.1:c.9108+774A= XP_011507631.1:n.9108+774A=
NM_002016.2:c.9882A= MANE Select NP_002007.1:p.Ala3294=