Canonical Allele Identifier: CA379108901
Gene: LSP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1887525T>C , CM000673.2:g.1887525T>C GRCh38
NC_000011.9:g.1908755T>C , CM000673.1:g.1908755T>C GRCh37
NC_000011.8:g.1865331T>C NCBI36
NG_011509.1:g.39556T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311604.8:c.982T>C MANE Select ENSP00000308383.4:p.Tyr328His
ENST00000311604.7:c.982T>C ENSP00000308383.3:p.Tyr328His
ENST00000381775.5:c.1366T>C ENSP00000371194.1:p.Tyr456His
ENST00000405957.6:c.796T>C ENSP00000383932.2:p.Tyr266His
ENST00000406638.6:c.796T>C ENSP00000384022.2:p.Tyr266His
ENST00000472974.5:n.852T>C
ENST00000485341.5:n.1478T>C
ENST00000612798.4:c.796T>C ENSP00000484140.1:p.Tyr266His
NM_001013253.1:c.796T>C NP_001013271.1:p.Tyr266His
NM_001013254.1:c.796T>C NP_001013272.1:p.Tyr266His
NM_001013255.1:c.796T>C NP_001013273.1:p.Tyr266His
NM_001242932.1:c.1366T>C NP_001229861.1:p.Tyr456His
NM_001289005.1:c.796T>C NP_001275934.1:p.Tyr266His
NM_002339.2:c.982T>C NP_002330.1:p.Tyr328His
NM_001013253.2:c.796T>C NP_001013271.1:p.Tyr266His
NM_002339.3:c.982T>C MANE Select NP_002330.1:p.Tyr328His
NM_001242932.2:c.1366T>C NP_001229861.1:p.Tyr456His
NM_001289005.2:c.796T>C NP_001275934.1:p.Tyr266His