Canonical Allele Identifier: CA889438545

Gene: FLG

Linked Data

• dbSNP Id: rs1342094625
• MyVariant Identifiers: chr1:g.152283336del (hg19) ; chr1:g.152310860del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152310860del , CM000663.2:g.152310860del	GRCh38
NC_000001.10:g.152283336del , CM000663.1:g.152283336del	GRCh37
NC_000001.9:g.150549960del	NCBI36
NG_016190.1:g.19344del , LRG_1028:g.19344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.4026del MANE Select	ENSP00000357789.1:p.Val1343CysfsTer?
ENST00000368799.1:c.4026del	ENSP00000357789.1:p.Val1343CysfsTer?
NM_002016.1:c.4026del , LRG_1028t1:c.4026del	NP_002007.1:p.Val1343CysfsTer?
XM_011509329.1:c.4026del	XP_011507631.1:p.Val1343CysfsTer?
NM_002016.2:c.4026del MANE Select	NP_002007.1:p.Val1343CysfsTer?