Canonical Allele Identifier: CA342070941
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304561C>T , CM000663.2:g.152304561C>T GRCh38
NC_000001.10:g.152277037C>T , CM000663.1:g.152277037C>T GRCh37
NC_000001.9:g.150543661C>T NCBI36
NG_016190.1:g.25643G>A , LRG_1028:g.25643G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10325G>A MANE Select ENSP00000357789.1:p.Arg3442Lys
ENST00000368799.1:c.10325G>A ENSP00000357789.1:p.Arg3442Lys
NM_002016.1:c.10325G>A , LRG_1028t1:c.10325G>A NP_002007.1:p.Arg3442Lys
XM_011509329.1:c.9109-728G>A XP_011507631.1:n.9109-728G>A
NM_002016.2:c.10325G>A MANE Select NP_002007.1:p.Arg3442Lys