Canonical Allele Identifier: CA379108851

Gene: LSP1

Linked Data

• COSMIC: COSM1168719 ; COSM1168720
• MyVariant Identifiers: chr11:g.1908732T>A (hg19) ; chr11:g.1887502T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887502T>A , CM000673.2:g.1887502T>A	GRCh38
NC_000011.9:g.1908732T>A , CM000673.1:g.1908732T>A	GRCh37
NC_000011.8:g.1865308T>A	NCBI36
NG_011509.1:g.39533T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.959T>A MANE Select	ENSP00000308383.4:p.Phe320Tyr
ENST00000311604.7:c.959T>A	ENSP00000308383.3:p.Phe320Tyr
ENST00000381775.5:c.1343T>A	ENSP00000371194.1:p.Phe448Tyr
ENST00000405957.6:c.773T>A	ENSP00000383932.2:p.Phe258Tyr
ENST00000406638.6:c.773T>A	ENSP00000384022.2:p.Phe258Tyr
ENST00000472974.5:n.829T>A
ENST00000484895.5:n.436T>A
ENST00000485341.5:n.1455T>A
ENST00000612798.4:c.773T>A	ENSP00000484140.1:p.Phe258Tyr
NM_001013253.1:c.773T>A	NP_001013271.1:p.Phe258Tyr
NM_001013254.1:c.773T>A	NP_001013272.1:p.Phe258Tyr
NM_001013255.1:c.773T>A	NP_001013273.1:p.Phe258Tyr
NM_001242932.1:c.1343T>A	NP_001229861.1:p.Phe448Tyr
NM_001289005.1:c.773T>A	NP_001275934.1:p.Phe258Tyr
NM_002339.2:c.959T>A	NP_002330.1:p.Phe320Tyr
NM_001013253.2:c.773T>A	NP_001013271.1:p.Phe258Tyr
NM_002339.3:c.959T>A MANE Select	NP_002330.1:p.Phe320Tyr
NM_001242932.2:c.1343T>A	NP_001229861.1:p.Phe448Tyr
NM_001289005.2:c.773T>A	NP_001275934.1:p.Phe258Tyr