Canonical Allele Identifier: CA597067920

Gene: LSP1

Linked Data

• dbSNP Id: rs1464330389
• gnomAD v2: 11-1909048-CT-C
• gnomAD v3: 11-1887818-CT-C
• gnomAD v4: 11-1887818-CT-C
• MyVariant Identifiers: chr11:g.1909049del (hg19) ; chr11:g.1887819del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887819del , CM000673.2:g.1887819del	GRCh38
NC_000011.9:g.1909049del , CM000673.1:g.1909049del	GRCh37
NC_000011.8:g.1865625del	NCBI36
NG_011509.1:g.39850del

Transcript Alleles

HGVS	Amino-acid change
ENST00000311604.8:c.*13+243del MANE Select	ENSP00000308383.4:n.*13+243del
ENST00000311604.7:c.*13+243del	ENSP00000308383.3:n.*13+243del
ENST00000381775.5:c.*13+243del	ENSP00000371194.1:n.*13+243del
ENST00000405957.6:c.*13+243del	ENSP00000383932.2:n.*13+243del
ENST00000406638.6:c.*13+243del	ENSP00000384022.2:n.*13+243del
ENST00000485341.5:n.1529+243del
ENST00000612798.4:c.*13+243del	ENSP00000484140.1:n.*13+243del
NM_001013253.1:c.*13+243del	NP_001013271.1:n.*13+243del
NM_001013254.1:c.*13+243del	NP_001013272.1:n.*13+243del
NM_001013255.1:c.*13+243del	NP_001013273.1:n.*13+243del
NM_001242932.1:c.*13+243del	NP_001229861.1:n.*13+243del
NM_001289005.1:c.*13+243del	NP_001275934.1:n.*13+243del
NM_002339.2:c.*13+243del	NP_002330.1:n.*13+243del
NM_001013253.2:c.*13+243del	NP_001013271.1:n.*13+243del
NM_002339.3:c.*13+243del MANE Select	NP_002330.1:n.*13+243del
NM_001242932.2:c.*13+243del	NP_001229861.1:n.*13+243del
NM_001289005.2:c.*13+243del	NP_001275934.1:n.*13+243del