Canonical Allele Identifier: CA674328799

Gene: LSP1

Linked Data

• dbSNP Id: rs1321500669
• gnomAD v4: 11-1887705-C-G
• MyVariant Identifiers: chr11:g.1908935C>G (hg19) ; chr11:g.1887705C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887705C>G , CM000673.2:g.1887705C>G	GRCh38
NC_000011.9:g.1908935C>G , CM000673.1:g.1908935C>G	GRCh37
NC_000011.8:g.1865511C>G	NCBI36
NG_011509.1:g.39736C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000311604.8:c.*13+129C>G MANE Select	ENSP00000308383.4:n.*13+129C>G
ENST00000311604.7:c.*13+129C>G	ENSP00000308383.3:n.*13+129C>G
ENST00000381775.5:c.*13+129C>G	ENSP00000371194.1:n.*13+129C>G
ENST00000405957.6:c.*13+129C>G	ENSP00000383932.2:n.*13+129C>G
ENST00000406638.6:c.*13+129C>G	ENSP00000384022.2:n.*13+129C>G
ENST00000485341.5:n.1529+129C>G
ENST00000612798.4:c.*13+129C>G	ENSP00000484140.1:n.*13+129C>G
NM_001013253.1:c.*13+129C>G	NP_001013271.1:n.*13+129C>G
NM_001013254.1:c.*13+129C>G	NP_001013272.1:n.*13+129C>G
NM_001013255.1:c.*13+129C>G	NP_001013273.1:n.*13+129C>G
NM_001242932.1:c.*13+129C>G	NP_001229861.1:n.*13+129C>G
NM_001289005.1:c.*13+129C>G	NP_001275934.1:n.*13+129C>G
NM_002339.2:c.*13+129C>G	NP_002330.1:n.*13+129C>G
NM_001013253.2:c.*13+129C>G	NP_001013271.1:n.*13+129C>G
NM_002339.3:c.*13+129C>G MANE Select	NP_002330.1:n.*13+129C>G
NM_001242932.2:c.*13+129C>G	NP_001229861.1:n.*13+129C>G
NM_001289005.2:c.*13+129C>G	NP_001275934.1:n.*13+129C>G