Canonical Allele Identifier: CA1141621044
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304671G= , CM000663.2:g.152304671G= GRCh38
NC_000001.10:g.152277147G= , CM000663.1:g.152277147G= GRCh37
NC_000001.9:g.150543771G= NCBI36
NG_016190.1:g.25533C= , LRG_1028:g.25533C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10215C= MANE Select ENSP00000357789.1:p.Thr3405=
ENST00000368799.1:c.10215C= ENSP00000357789.1:p.Thr3405=
NM_002016.1:c.10215C= , LRG_1028t1:c.10215C= NP_002007.1:p.Thr3405=
XM_011509329.1:c.9109-838C= XP_011507631.1:n.9109-838C=
NM_002016.2:c.10215C= MANE Select NP_002007.1:p.Thr3405=