Canonical Allele Identifier: CA1947897085

Gene: LSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887552C= , CM000673.2:g.1887552C=	GRCh38
NC_000011.9:g.1908782C= , CM000673.1:g.1908782C=	GRCh37
NC_000011.8:g.1865358C=	NCBI36
NG_011509.1:g.39583C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.1009C= MANE Select	ENSP00000308383.4:p.Pro337=
ENST00000311604.7:c.1009C=	ENSP00000308383.3:p.Pro337=
ENST00000381775.5:c.1393C=	ENSP00000371194.1:p.Pro465=
ENST00000405957.6:c.823C=	ENSP00000383932.2:p.Pro275=
ENST00000406638.6:c.823C=	ENSP00000384022.2:p.Pro275=
ENST00000472974.5:n.879C=
ENST00000485341.5:n.1505C=
ENST00000612798.4:c.823C=	ENSP00000484140.1:p.Pro275=
NM_001013253.1:c.823C=	NP_001013271.1:p.Pro275=
NM_001013254.1:c.823C=	NP_001013272.1:p.Pro275=
NM_001013255.1:c.823C=	NP_001013273.1:p.Pro275=
NM_001242932.1:c.1393C=	NP_001229861.1:p.Pro465=
NM_001289005.1:c.823C=	NP_001275934.1:p.Pro275=
NM_002339.2:c.1009C=	NP_002330.1:p.Pro337=
NM_001013253.2:c.823C=	NP_001013271.1:p.Pro275=
NM_002339.3:c.1009C= MANE Select	NP_002330.1:p.Pro337=
NM_001242932.2:c.1393C=	NP_001229861.1:p.Pro465=
NM_001289005.2:c.823C=	NP_001275934.1:p.Pro275=