Canonical Allele Identifier: CA1947897077
Gene: LSP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1887540G= , CM000673.2:g.1887540G= GRCh38
NC_000011.9:g.1908770G= , CM000673.1:g.1908770G= GRCh37
NC_000011.8:g.1865346G= NCBI36
NG_011509.1:g.39571G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311604.8:c.997G= MANE Select ENSP00000308383.4:p.Val333=
ENST00000311604.7:c.997G= ENSP00000308383.3:p.Val333=
ENST00000381775.5:c.1381G= ENSP00000371194.1:p.Val461=
ENST00000405957.6:c.811G= ENSP00000383932.2:p.Val271=
ENST00000406638.6:c.811G= ENSP00000384022.2:p.Val271=
ENST00000472974.5:n.867G=
ENST00000485341.5:n.1493G=
ENST00000612798.4:c.811G= ENSP00000484140.1:p.Val271=
NM_001013253.1:c.811G= NP_001013271.1:p.Val271=
NM_001013254.1:c.811G= NP_001013272.1:p.Val271=
NM_001013255.1:c.811G= NP_001013273.1:p.Val271=
NM_001242932.1:c.1381G= NP_001229861.1:p.Val461=
NM_001289005.1:c.811G= NP_001275934.1:p.Val271=
NM_002339.2:c.997G= NP_002330.1:p.Val333=
NM_001013253.2:c.811G= NP_001013271.1:p.Val271=
NM_002339.3:c.997G= MANE Select NP_002330.1:p.Val333=
NM_001242932.2:c.1381G= NP_001229861.1:p.Val461=
NM_001289005.2:c.811G= NP_001275934.1:p.Val271=