Canonical Allele Identifier: CA13435612
Gene: LSP1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3817198

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1887776T>C , CM000673.2:g.1887776T>C GRCh38
NC_000011.9:g.1909006T>C , CM000673.1:g.1909006T>C GRCh37
NC_000011.8:g.1865582T>C NCBI36
NG_011509.1:g.39807T>C

Transcript Alleles

HGVS Amino-acid change
NM_001013253.1:c.*13+200T>C VV NP_001013271.1:p.=
NM_001013254.1:c.*13+200T>C VV NP_001013272.1:p.=
NM_001013255.1:c.*13+200T>C VV NP_001013273.1:p.=
NM_001242932.1:c.*13+200T>C VV NP_001229861.1:p.=
NM_001289005.1:c.*13+200T>C VV NP_001275934.1:p.=
NM_002339.2:c.*13+200T>C VV NP_002330.1:p.=
ENST00000311604.7:c.*13+200T>C ENSP00000308383.3:p.=
ENST00000381775.5:c.*13+200T>C ENSP00000371194.1:p.=
ENST00000405957.6:c.*13+200T>C ENSP00000383932.2:p.=
ENST00000406638.6:c.*13+200T>C ENSP00000384022.2:p.=
ENST00000485341.5:n.1529+200T>C
ENST00000612798.4:c.*13+200T>C ENSP00000484140.1:p.=