Canonical Allele Identifier: CA1141880848
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311266G= , CM000663.2:g.152311266G= GRCh38
NC_000001.10:g.152283742G= , CM000663.1:g.152283742G= GRCh37
NC_000001.9:g.150550366G= NCBI36
NG_016190.1:g.18938C= , LRG_1028:g.18938C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3620C= MANE Select ENSP00000357789.1:p.Ser1207=
ENST00000368799.1:c.3620C= ENSP00000357789.1:p.Ser1207=
NM_002016.1:c.3620C= , LRG_1028t1:c.3620C= NP_002007.1:p.Ser1207=
XM_011509329.1:c.3620C= XP_011507631.1:p.Ser1207=
NM_002016.2:c.3620C= MANE Select NP_002007.1:p.Ser1207=