Canonical Allele Identifier: CA1947897072

Gene: LSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887529A= , CM000673.2:g.1887529A=	GRCh38
NC_000011.9:g.1908759A= , CM000673.1:g.1908759A=	GRCh37
NC_000011.8:g.1865335A=	NCBI36
NG_011509.1:g.39560A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.986A= MANE Select	ENSP00000308383.4:p.Glu329=
ENST00000311604.7:c.986A=	ENSP00000308383.3:p.Glu329=
ENST00000381775.5:c.1370A=	ENSP00000371194.1:p.Glu457=
ENST00000405957.6:c.800A=	ENSP00000383932.2:p.Glu267=
ENST00000406638.6:c.800A=	ENSP00000384022.2:p.Glu267=
ENST00000472974.5:n.856A=
ENST00000485341.5:n.1482A=
ENST00000612798.4:c.800A=	ENSP00000484140.1:p.Glu267=
NM_001013253.1:c.800A=	NP_001013271.1:p.Glu267=
NM_001013254.1:c.800A=	NP_001013272.1:p.Glu267=
NM_001013255.1:c.800A=	NP_001013273.1:p.Glu267=
NM_001242932.1:c.1370A=	NP_001229861.1:p.Glu457=
NM_001289005.1:c.800A=	NP_001275934.1:p.Glu267=
NM_002339.2:c.986A=	NP_002330.1:p.Glu329=
NM_001013253.2:c.800A=	NP_001013271.1:p.Glu267=
NM_002339.3:c.986A= MANE Select	NP_002330.1:p.Glu329=
NM_001242932.2:c.1370A=	NP_001229861.1:p.Glu457=
NM_001289005.2:c.800A=	NP_001275934.1:p.Glu267=