Canonical Allele Identifier: CA471993602

Gene: LSP1

Linked Data

• MyVariant Identifiers: chr11:g.1908766G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887536G>C , CM000673.2:g.1887536G>C	GRCh38
NC_000011.9:g.1908766G>C , CM000673.1:g.1908766G>C	GRCh37
NC_000011.8:g.1865342G>C	NCBI36
NG_011509.1:g.39567G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.993G>C MANE Select	ENSP00000308383.4:p.Val331=
ENST00000311604.7:c.993G>C	ENSP00000308383.3:p.Val331=
ENST00000381775.5:c.1377G>C	ENSP00000371194.1:p.Val459=
ENST00000405957.6:c.807G>C	ENSP00000383932.2:p.Val269=
ENST00000406638.6:c.807G>C	ENSP00000384022.2:p.Val269=
ENST00000472974.5:n.863G>C
ENST00000485341.5:n.1489G>C
ENST00000612798.4:c.807G>C	ENSP00000484140.1:p.Val269=
NM_001013253.1:c.807G>C	NP_001013271.1:p.Val269=
NM_001013254.1:c.807G>C	NP_001013272.1:p.Val269=
NM_001013255.1:c.807G>C	NP_001013273.1:p.Val269=
NM_001242932.1:c.1377G>C	NP_001229861.1:p.Val459=
NM_001289005.1:c.807G>C	NP_001275934.1:p.Val269=
NM_002339.2:c.993G>C	NP_002330.1:p.Val331=
NM_001013253.2:c.807G>C	NP_001013271.1:p.Val269=
NM_002339.3:c.993G>C MANE Select	NP_002330.1:p.Val331=
NM_001242932.2:c.1377G>C	NP_001229861.1:p.Val459=
NM_001289005.2:c.807G>C	NP_001275934.1:p.Val269=