Canonical Allele Identifier: CA2479951289
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311291T= , CM000663.2:g.152311291T= GRCh38
NC_000001.10:g.152283767T= , CM000663.1:g.152283767T= GRCh37
NC_000001.9:g.150550391T= NCBI36
NG_016190.1:g.18913A= , LRG_1028:g.18913A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3595A= MANE Select ENSP00000357789.1:p.Thr1199=
ENST00000368799.1:c.3595A= ENSP00000357789.1:p.Thr1199=
NM_002016.1:c.3595A= , LRG_1028t1:c.3595A= NP_002007.1:p.Thr1199=
XM_011509329.1:c.3595A= XP_011507631.1:p.Thr1199=
NM_002016.2:c.3595A= MANE Select NP_002007.1:p.Thr1199=