Canonical Allele Identifier: CA597067884
Gene: LSP1 HGNC NCBI

Linked Data

dbSNP Id: rs1326262653
gnomAD v2: 11-1908956-A-G
gnomAD v3: 11-1887726-A-G
gnomAD v4: 11-1887726-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1887726A>G , CM000673.2:g.1887726A>G GRCh38
NC_000011.9:g.1908956A>G , CM000673.1:g.1908956A>G GRCh37
NC_000011.8:g.1865532A>G NCBI36
NG_011509.1:g.39757A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000311604.8:c.*13+150A>G MANE Select ENSP00000308383.4:n.*13+150A>G
ENST00000311604.7:c.*13+150A>G ENSP00000308383.3:n.*13+150A>G
ENST00000381775.5:c.*13+150A>G ENSP00000371194.1:n.*13+150A>G
ENST00000405957.6:c.*13+150A>G ENSP00000383932.2:n.*13+150A>G
ENST00000406638.6:c.*13+150A>G ENSP00000384022.2:n.*13+150A>G
ENST00000485341.5:n.1529+150A>G
ENST00000612798.4:c.*13+150A>G ENSP00000484140.1:n.*13+150A>G
NM_001013253.1:c.*13+150A>G NP_001013271.1:n.*13+150A>G
NM_001013254.1:c.*13+150A>G NP_001013272.1:n.*13+150A>G
NM_001013255.1:c.*13+150A>G NP_001013273.1:n.*13+150A>G
NM_001242932.1:c.*13+150A>G NP_001229861.1:n.*13+150A>G
NM_001289005.1:c.*13+150A>G NP_001275934.1:n.*13+150A>G
NM_002339.2:c.*13+150A>G NP_002330.1:n.*13+150A>G
NM_001013253.2:c.*13+150A>G NP_001013271.1:n.*13+150A>G
NM_002339.3:c.*13+150A>G MANE Select NP_002330.1:n.*13+150A>G
NM_001242932.2:c.*13+150A>G NP_001229861.1:n.*13+150A>G
NM_001289005.2:c.*13+150A>G NP_001275934.1:n.*13+150A>G