Canonical Allele Identifier: CA889442010

Gene: FLG

Linked Data

• dbSNP Id: rs1188191297
• MyVariant Identifiers: chr1:g.152284720_152284725del (hg19) ; chr1:g.152312244_152312249del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152312244_152312249del , CM000663.2:g.152312244_152312249del	GRCh38
NC_000001.10:g.152284720_152284725del , CM000663.1:g.152284720_152284725del	GRCh37
NC_000001.9:g.150551344_150551349del	NCBI36
NG_016190.1:g.17955_17960del , LRG_1028:g.17955_17960del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.2637_2642del MANE Select	ENSP00000357789.1:p.Arg879_Asp881delinsSer
ENST00000368799.1:c.2637_2642del	ENSP00000357789.1:p.Arg879_Asp881delinsSer
NM_002016.1:c.2637_2642del , LRG_1028t1:c.2637_2642del	NP_002007.1:p.Arg879_Asp881delinsSer
XM_011509329.1:c.2637_2642del	XP_011507631.1:p.Arg879_Asp881delinsSer
NM_002016.2:c.2637_2642del MANE Select	NP_002007.1:p.Arg879_Asp881delinsSer