Canonical Allele Identifier: CA934407099

Gene: LSP1

Linked Data

• dbSNP Id: rs1848812270

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887608_1887611dup , CM000673.2:g.1887608_1887611dup	GRCh38
NC_000011.9:g.1908838_1908841dup , CM000673.1:g.1908838_1908841dup	GRCh37
NC_000011.8:g.1865414_1865417dup	NCBI36
NG_011509.1:g.39639_39642dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.*13+32_*13+35dup MANE Select	ENSP00000308383.4:n.*13+32_*13+35dup
ENST00000311604.7:c.*13+32_*13+35dup	ENSP00000308383.3:n.*13+32_*13+35dup
ENST00000381775.5:c.*13+32_*13+35dup	ENSP00000371194.1:n.*13+32_*13+35dup
ENST00000405957.6:c.*13+32_*13+35dup	ENSP00000383932.2:n.*13+32_*13+35dup
ENST00000406638.6:c.*13+32_*13+35dup	ENSP00000384022.2:n.*13+32_*13+35dup
ENST00000485341.5:n.1529+32_1529+35dup
ENST00000612798.4:c.*13+32_*13+35dup	ENSP00000484140.1:n.*13+32_*13+35dup
NM_001013253.1:c.*13+32_*13+35dup	NP_001013271.1:n.*13+32_*13+35dup
NM_001013254.1:c.*13+32_*13+35dup	NP_001013272.1:n.*13+32_*13+35dup
NM_001013255.1:c.*13+32_*13+35dup	NP_001013273.1:n.*13+32_*13+35dup
NM_001242932.1:c.*13+32_*13+35dup	NP_001229861.1:n.*13+32_*13+35dup
NM_001289005.1:c.*13+32_*13+35dup	NP_001275934.1:n.*13+32_*13+35dup
NM_002339.2:c.*13+32_*13+35dup	NP_002330.1:n.*13+32_*13+35dup
NM_001013253.2:c.*13+32_*13+35dup	NP_001013271.1:n.*13+32_*13+35dup
NM_002339.3:c.*13+32_*13+35dup MANE Select	NP_002330.1:n.*13+32_*13+35dup
NM_001242932.2:c.*13+32_*13+35dup	NP_001229861.1:n.*13+32_*13+35dup
NM_001289005.2:c.*13+32_*13+35dup	NP_001275934.1:n.*13+32_*13+35dup