Canonical Allele Identifier: CA420928929

Gene: FLG

Linked Data

• COSMIC: COSM1600823
• MyVariant Identifiers: chr1:g.152281093del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152308619del , CM000663.2:g.152308619del	GRCh38
NC_000001.10:g.152281095del , CM000663.1:g.152281095del	GRCh37
NC_000001.9:g.150547719del	NCBI36
NG_016190.1:g.21587del , LRG_1028:g.21587del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.6269del MANE Select	ENSP00000357789.1:p.Phe2090SerfsTer5
ENST00000368799.1:c.6269del	ENSP00000357789.1:p.Phe2090SerfsTer5
NM_002016.1:c.6269del , LRG_1028t1:c.6269del	NP_002007.1:p.Phe2090SerfsTer5
XM_011509329.1:c.6269del	XP_011507631.1:p.Phe2090SerfsTer5
NM_002016.2:c.6269del MANE Select	NP_002007.1:p.Phe2090SerfsTer5