Canonical Allele Identifier: CA2586967289
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309214_152309215delinsTA , CM000663.2:g.152309214_152309215delinsTA GRCh38
NC_000001.10:g.152281690_152281691delinsTA , CM000663.1:g.152281690_152281691delinsTA GRCh37
NC_000001.9:g.150548314_150548315delinsTA NCBI36
NG_016190.1:g.20989_20990delinsTA , LRG_1028:g.20989_20990delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5671_5672delinsTA MANE Select ENSP00000357789.1:p.Arg1891Ter
ENST00000368799.1:c.5671_5672delinsTA ENSP00000357789.1:p.Arg1891Ter
NM_002016.1:c.5671_5672delinsTA , LRG_1028t1:c.5671_5672delinsTA NP_002007.1:p.Arg1891Ter
XM_011509329.1:c.5671_5672delinsTA XP_011507631.1:p.Arg1891Ter
NM_002016.2:c.5671_5672delinsTA MANE Select NP_002007.1:p.Arg1891Ter