Canonical Allele Identifier: CA2647993492
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304391_152304508del , CM000663.2:g.152304391_152304508del GRCh38
NC_000001.10:g.152276867_152276984del , CM000663.1:g.152276867_152276984del GRCh37
NC_000001.9:g.150543491_150543608del NCBI36
NG_016190.1:g.25696_25813del , LRG_1028:g.25696_25813del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10378_10495del MANE Select ENSP00000357789.1:p.Ser3460ProfsTer?
ENST00000368799.1:c.10378_10495del ENSP00000357789.1:p.Ser3460ProfsTer?
NM_002016.1:c.10378_10495del , LRG_1028t1:c.10378_10495del NP_002007.1:p.Ser3460ProfsTer?
XM_011509329.1:c.9109-675_9109-558del XP_011507631.1:n.9109-675_9109-558del
NM_002016.2:c.10378_10495del MANE Select NP_002007.1:p.Ser3460ProfsTer?