Canonical Allele Identifier: CA379108962

Gene: LSP1

Linked Data

• COSMIC: COSM6132308 ; COSM6132309
• MyVariant Identifiers: chr11:g.1908785G>T (hg19) ; chr11:g.1887555G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887555G>T , CM000673.2:g.1887555G>T	GRCh38
NC_000011.9:g.1908785G>T , CM000673.1:g.1908785G>T	GRCh37
NC_000011.8:g.1865361G>T	NCBI36
NG_011509.1:g.39586G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.1012G>T MANE Select	ENSP00000308383.4:p.Ala338Ser
ENST00000311604.7:c.1012G>T	ENSP00000308383.3:p.Ala338Ser
ENST00000381775.5:c.1396G>T	ENSP00000371194.1:p.Ala466Ser
ENST00000405957.6:c.826G>T	ENSP00000383932.2:p.Ala276Ser
ENST00000406638.6:c.826G>T	ENSP00000384022.2:p.Ala276Ser
ENST00000472974.5:n.882G>T
ENST00000485341.5:n.1508G>T
ENST00000612798.4:c.826G>T	ENSP00000484140.1:p.Ala276Ser
NM_001013253.1:c.826G>T	NP_001013271.1:p.Ala276Ser
NM_001013254.1:c.826G>T	NP_001013272.1:p.Ala276Ser
NM_001013255.1:c.826G>T	NP_001013273.1:p.Ala276Ser
NM_001242932.1:c.1396G>T	NP_001229861.1:p.Ala466Ser
NM_001289005.1:c.826G>T	NP_001275934.1:p.Ala276Ser
NM_002339.2:c.1012G>T	NP_002330.1:p.Ala338Ser
NM_001013253.2:c.826G>T	NP_001013271.1:p.Ala276Ser
NM_002339.3:c.1012G>T MANE Select	NP_002330.1:p.Ala338Ser
NM_001242932.2:c.1396G>T	NP_001229861.1:p.Ala466Ser
NM_001289005.2:c.826G>T	NP_001275934.1:p.Ala276Ser