Canonical Allele Identifier: CA5815898

Gene: LSP1

Linked Data

• dbSNP Id: rs753967969
• ExAC: 11:1908842 GCA / G
• gnomAD v2: 11-1908842-GCA-G
• gnomAD v4: 11-1887612-GCA-G
• MyVariant Identifiers: chr11:g.1908843_1908844del (hg19) ; chr11:g.1887613_1887614del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887618_1887619del , CM000673.2:g.1887618_1887619del	GRCh38
NC_000011.9:g.1908848_1908849del , CM000673.1:g.1908848_1908849del	GRCh37
NC_000011.8:g.1865424_1865425del	NCBI36
NG_011509.1:g.39649_39650del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.*13+42_*13+43del MANE Select	ENSP00000308383.4:n.*13+42_*13+43del
ENST00000311604.7:c.*13+42_*13+43del	ENSP00000308383.3:n.*13+42_*13+43del
ENST00000381775.5:c.*13+42_*13+43del	ENSP00000371194.1:n.*13+42_*13+43del
ENST00000405957.6:c.*13+42_*13+43del	ENSP00000383932.2:n.*13+42_*13+43del
ENST00000406638.6:c.*13+42_*13+43del	ENSP00000384022.2:n.*13+42_*13+43del
ENST00000485341.5:n.1529+42_1529+43del
ENST00000612798.4:c.*13+42_*13+43del	ENSP00000484140.1:n.*13+42_*13+43del
NM_001013253.1:c.*13+42_*13+43del	NP_001013271.1:n.*13+42_*13+43del
NM_001013254.1:c.*13+42_*13+43del	NP_001013272.1:n.*13+42_*13+43del
NM_001013255.1:c.*13+42_*13+43del	NP_001013273.1:n.*13+42_*13+43del
NM_001242932.1:c.*13+42_*13+43del	NP_001229861.1:n.*13+42_*13+43del
NM_001289005.1:c.*13+42_*13+43del	NP_001275934.1:n.*13+42_*13+43del
NM_002339.2:c.*13+42_*13+43del	NP_002330.1:n.*13+42_*13+43del
NM_001013253.2:c.*13+42_*13+43del	NP_001013271.1:n.*13+42_*13+43del
NM_002339.3:c.*13+42_*13+43del MANE Select	NP_002330.1:n.*13+42_*13+43del
NM_001242932.2:c.*13+42_*13+43del	NP_001229861.1:n.*13+42_*13+43del
NM_001289005.2:c.*13+42_*13+43del	NP_001275934.1:n.*13+42_*13+43del