Canonical Allele Identifier: CA2479949884
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308761C= , CM000663.2:g.152308761C= GRCh38
NC_000001.10:g.152281237C= , CM000663.1:g.152281237C= GRCh37
NC_000001.9:g.150547861C= NCBI36
NG_016190.1:g.21443G= , LRG_1028:g.21443G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6125G= MANE Select ENSP00000357789.1:p.Ser2042=
ENST00000368799.1:c.6125G= ENSP00000357789.1:p.Ser2042=
NM_002016.1:c.6125G= , LRG_1028t1:c.6125G= NP_002007.1:p.Ser2042=
XM_011509329.1:c.6125G= XP_011507631.1:p.Ser2042=
NM_002016.2:c.6125G= MANE Select NP_002007.1:p.Ser2042=