Canonical Allele Identifier: CA379108923

Gene: LSP1

Linked Data

• MyVariant Identifiers: chr11:g.1908764G>A (hg19) ; chr11:g.1887534G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887534G>A , CM000673.2:g.1887534G>A	GRCh38
NC_000011.9:g.1908764G>A , CM000673.1:g.1908764G>A	GRCh37
NC_000011.8:g.1865340G>A	NCBI36
NG_011509.1:g.39565G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.991G>A MANE Select	ENSP00000308383.4:p.Val331Met
ENST00000311604.7:c.991G>A	ENSP00000308383.3:p.Val331Met
ENST00000381775.5:c.1375G>A	ENSP00000371194.1:p.Val459Met
ENST00000405957.6:c.805G>A	ENSP00000383932.2:p.Val269Met
ENST00000406638.6:c.805G>A	ENSP00000384022.2:p.Val269Met
ENST00000472974.5:n.861G>A
ENST00000485341.5:n.1487G>A
ENST00000612798.4:c.805G>A	ENSP00000484140.1:p.Val269Met
NM_001013253.1:c.805G>A	NP_001013271.1:p.Val269Met
NM_001013254.1:c.805G>A	NP_001013272.1:p.Val269Met
NM_001013255.1:c.805G>A	NP_001013273.1:p.Val269Met
NM_001242932.1:c.1375G>A	NP_001229861.1:p.Val459Met
NM_001289005.1:c.805G>A	NP_001275934.1:p.Val269Met
NM_002339.2:c.991G>A	NP_002330.1:p.Val331Met
NM_001013253.2:c.805G>A	NP_001013271.1:p.Val269Met
NM_002339.3:c.991G>A MANE Select	NP_002330.1:p.Val331Met
NM_001242932.2:c.1375G>A	NP_001229861.1:p.Val459Met
NM_001289005.2:c.805G>A	NP_001275934.1:p.Val269Met