Canonical Allele Identifier: CA2479947613
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304747G= , CM000663.2:g.152304747G= GRCh38
NC_000001.10:g.152277223G= , CM000663.1:g.152277223G= GRCh37
NC_000001.9:g.150543847G= NCBI36
NG_016190.1:g.25457C= , LRG_1028:g.25457C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10139C= MANE Select ENSP00000357789.1:p.Ser3380=
ENST00000368799.1:c.10139C= ENSP00000357789.1:p.Ser3380=
NM_002016.1:c.10139C= , LRG_1028t1:c.10139C= NP_002007.1:p.Ser3380=
XM_011509329.1:c.9109-914C= XP_011507631.1:n.9109-914C=
NM_002016.2:c.10139C= MANE Select NP_002007.1:p.Ser3380=