Canonical Allele Identifier: CA2479947804
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305065G= , CM000663.2:g.152305065G= GRCh38
NC_000001.10:g.152277541G= , CM000663.1:g.152277541G= GRCh37
NC_000001.9:g.150544165G= NCBI36
NG_016190.1:g.25139C= , LRG_1028:g.25139C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9821C= MANE Select ENSP00000357789.1:p.Ser3274=
ENST00000368799.1:c.9821C= ENSP00000357789.1:p.Ser3274=
NM_002016.1:c.9821C= , LRG_1028t1:c.9821C= NP_002007.1:p.Ser3274=
XM_011509329.1:c.9108+713C= XP_011507631.1:n.9108+713C=
NM_002016.2:c.9821C= MANE Select NP_002007.1:p.Ser3274=