Canonical Allele Identifier: CA2479950130
Gene: FLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309183_152309187delinsGCCCA , CM000663.2:g.152309183_152309187delinsGCCCA GRCh38
NC_000001.10:g.152281659_152281663delinsGCCCA , CM000663.1:g.152281659_152281663delinsGCCCA GRCh37
NC_000001.9:g.150548283_150548287delinsGCCCA NCBI36
NG_016190.1:g.21017_21021delinsTGGGC , LRG_1028:g.21017_21021delinsTGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5699_5703delinsTGGGC MANE Select ENSP00000357789.1:p.Val1900=
ENST00000368799.1:c.5699_5703delinsTGGGC ENSP00000357789.1:p.Val1900=
NM_002016.1:c.5699_5703delinsTGGGC , LRG_1028t1:c.5699_5703delinsTGGGC NP_002007.1:p.Val1900=
XM_011509329.1:c.5699_5703delinsTGGGC XP_011507631.1:p.Val1900=
NM_002016.2:c.5699_5703delinsTGGGC MANE Select NP_002007.1:p.Val1900=