Canonical Allele Identifier: CA2647993619
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311056del , CM000663.2:g.152311056del GRCh38
NC_000001.10:g.152283532del , CM000663.1:g.152283532del GRCh37
NC_000001.9:g.150550156del NCBI36
NG_016190.1:g.19148del , LRG_1028:g.19148del

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.3830del MANE Select ENSP00000357789.1:p.Glu1277GlyfsTer?
ENST00000368799.1:c.3830del ENSP00000357789.1:p.Glu1277GlyfsTer?
NM_002016.1:c.3830del , LRG_1028t1:c.3830del NP_002007.1:p.Glu1277GlyfsTer?
XM_011509329.1:c.3830del XP_011507631.1:p.Glu1277GlyfsTer?
NM_002016.2:c.3830del MANE Select NP_002007.1:p.Glu1277GlyfsTer?