Canonical Allele Identifier: CA1947897089

Gene: LSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887557T= , CM000673.2:g.1887557T=	GRCh38
NC_000011.9:g.1908787T= , CM000673.1:g.1908787T=	GRCh37
NC_000011.8:g.1865363T=	NCBI36
NG_011509.1:g.39588T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.1014T= MANE Select	ENSP00000308383.4:p.Ala338=
ENST00000311604.7:c.1014T=	ENSP00000308383.3:p.Ala338=
ENST00000381775.5:c.1398T=	ENSP00000371194.1:p.Ala466=
ENST00000405957.6:c.828T=	ENSP00000383932.2:p.Ala276=
ENST00000406638.6:c.828T=	ENSP00000384022.2:p.Ala276=
ENST00000472974.5:n.884T=
ENST00000485341.5:n.1510T=
ENST00000612798.4:c.828T=	ENSP00000484140.1:p.Ala276=
NM_001013253.1:c.828T=	NP_001013271.1:p.Ala276=
NM_001013254.1:c.828T=	NP_001013272.1:p.Ala276=
NM_001013255.1:c.828T=	NP_001013273.1:p.Ala276=
NM_001242932.1:c.1398T=	NP_001229861.1:p.Ala466=
NM_001289005.1:c.828T=	NP_001275934.1:p.Ala276=
NM_002339.2:c.1014T=	NP_002330.1:p.Ala338=
NM_001013253.2:c.828T=	NP_001013271.1:p.Ala276=
NM_002339.3:c.1014T= MANE Select	NP_002330.1:p.Ala338=
NM_001242932.2:c.1398T=	NP_001229861.1:p.Ala466=
NM_001289005.2:c.828T=	NP_001275934.1:p.Ala276=