Canonical Allele Identifier: CA379108875

Gene: LSP1

Linked Data

• MyVariant Identifiers: chr11:g.1908744G>C (hg19) ; chr11:g.1887514G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887514G>C , CM000673.2:g.1887514G>C	GRCh38
NC_000011.9:g.1908744G>C , CM000673.1:g.1908744G>C	GRCh37
NC_000011.8:g.1865320G>C	NCBI36
NG_011509.1:g.39545G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.971G>C MANE Select	ENSP00000308383.4:p.Gly324Ala
ENST00000311604.7:c.971G>C	ENSP00000308383.3:p.Gly324Ala
ENST00000381775.5:c.1355G>C	ENSP00000371194.1:p.Gly452Ala
ENST00000405957.6:c.785G>C	ENSP00000383932.2:p.Gly262Ala
ENST00000406638.6:c.785G>C	ENSP00000384022.2:p.Gly262Ala
ENST00000472974.5:n.841G>C
ENST00000485341.5:n.1467G>C
ENST00000612798.4:c.785G>C	ENSP00000484140.1:p.Gly262Ala
NM_001013253.1:c.785G>C	NP_001013271.1:p.Gly262Ala
NM_001013254.1:c.785G>C	NP_001013272.1:p.Gly262Ala
NM_001013255.1:c.785G>C	NP_001013273.1:p.Gly262Ala
NM_001242932.1:c.1355G>C	NP_001229861.1:p.Gly452Ala
NM_001289005.1:c.785G>C	NP_001275934.1:p.Gly262Ala
NM_002339.2:c.971G>C	NP_002330.1:p.Gly324Ala
NM_001013253.2:c.785G>C	NP_001013271.1:p.Gly262Ala
NM_002339.3:c.971G>C MANE Select	NP_002330.1:p.Gly324Ala
NM_001242932.2:c.1355G>C	NP_001229861.1:p.Gly452Ala
NM_001289005.2:c.785G>C	NP_001275934.1:p.Gly262Ala