Canonical Allele Identifier: CA2647993557
Gene: FLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310509_152310512del , CM000663.2:g.152310509_152310512del GRCh38
NC_000001.10:g.152282985_152282988del , CM000663.1:g.152282985_152282988del GRCh37
NC_000001.9:g.150549609_150549612del NCBI36
NG_016190.1:g.19692_19695del , LRG_1028:g.19692_19695del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4374_4377del MANE Select ENSP00000357789.1:p.Ala1459ProfsTer?
ENST00000368799.1:c.4374_4377del ENSP00000357789.1:p.Ala1459ProfsTer?
NM_002016.1:c.4374_4377del , LRG_1028t1:c.4374_4377del NP_002007.1:p.Ala1459ProfsTer?
XM_011509329.1:c.4374_4377del XP_011507631.1:p.Ala1459ProfsTer?
NM_002016.2:c.4374_4377del MANE Select NP_002007.1:p.Ala1459ProfsTer?