Canonical Allele Identifier: CA2479952771
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152314002G= , CM000663.2:g.152314002G= GRCh38
NC_000001.10:g.152286478G= , CM000663.1:g.152286478G= GRCh37
NC_000001.9:g.150553102G= NCBI36
NG_016190.1:g.16202C= , LRG_1028:g.16202C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.884C= MANE Select ENSP00000357789.1:p.Ser295=
ENST00000368799.1:c.884C= ENSP00000357789.1:p.Ser295=
NM_002016.1:c.884C= , LRG_1028t1:c.884C= NP_002007.1:p.Ser295=
NR_103778.1:n.544G=
XM_011509329.1:c.884C= XP_011507631.1:p.Ser295=
NM_002016.2:c.884C= MANE Select NP_002007.1:p.Ser295=