Canonical Allele Identifier: CA889442304

Gene: FLG

Linked Data

• dbSNP Id: rs1296242247
• MyVariant Identifiers: chr1:g.152284828del (hg19) ; chr1:g.152312352del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152312354del , CM000663.2:g.152312354del	GRCh38
NC_000001.10:g.152284830del , CM000663.1:g.152284830del	GRCh37
NC_000001.9:g.150551454del	NCBI36
NG_016190.1:g.17852del , LRG_1028:g.17852del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.2534del MANE Select	ENSP00000357789.1:p.Pro845ArgfsTer17
ENST00000368799.1:c.2534del	ENSP00000357789.1:p.Pro845ArgfsTer17
NM_002016.1:c.2534del , LRG_1028t1:c.2534del	NP_002007.1:p.Pro845ArgfsTer17
XM_011509329.1:c.2534del	XP_011507631.1:p.Pro845ArgfsTer17
NM_002016.2:c.2534del MANE Select	NP_002007.1:p.Pro845ArgfsTer17