Canonical Allele Identifier: CA471993573

Gene: LSP1

Linked Data

• MyVariant Identifiers: chr11:g.1908715T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887485T>A , CM000673.2:g.1887485T>A	GRCh38
NC_000011.9:g.1908715T>A , CM000673.1:g.1908715T>A	GRCh37
NC_000011.8:g.1865291T>A	NCBI36
NG_011509.1:g.39516T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.942T>A MANE Select	ENSP00000308383.4:p.Ser314=
ENST00000311604.7:c.942T>A	ENSP00000308383.3:p.Ser314=
ENST00000381775.5:c.1326T>A	ENSP00000371194.1:p.Ser442=
ENST00000405957.6:c.756T>A	ENSP00000383932.2:p.Ser252=
ENST00000406638.6:c.756T>A	ENSP00000384022.2:p.Ser252=
ENST00000472974.5:n.812T>A
ENST00000484895.5:n.419T>A
ENST00000485341.5:n.1438T>A
ENST00000612798.4:c.756T>A	ENSP00000484140.1:p.Ser252=
NM_001013253.1:c.756T>A	NP_001013271.1:p.Ser252=
NM_001013254.1:c.756T>A	NP_001013272.1:p.Ser252=
NM_001013255.1:c.756T>A	NP_001013273.1:p.Ser252=
NM_001242932.1:c.1326T>A	NP_001229861.1:p.Ser442=
NM_001289005.1:c.756T>A	NP_001275934.1:p.Ser252=
NM_002339.2:c.942T>A	NP_002330.1:p.Ser314=
NM_001013253.2:c.756T>A	NP_001013271.1:p.Ser252=
NM_002339.3:c.942T>A MANE Select	NP_002330.1:p.Ser314=
NM_001242932.2:c.1326T>A	NP_001229861.1:p.Ser442=
NM_001289005.2:c.756T>A	NP_001275934.1:p.Ser252=