Canonical Allele Identifier: CA1947897210

Gene: LSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887797C= , CM000673.2:g.1887797C=	GRCh38
NC_000011.9:g.1909027C= , CM000673.1:g.1909027C=	GRCh37
NC_000011.8:g.1865603C=	NCBI36
NG_011509.1:g.39828C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311604.8:c.*13+221C= MANE Select	ENSP00000308383.4:n.*13+221C=
ENST00000311604.7:c.*13+221C=	ENSP00000308383.3:n.*13+221C=
ENST00000381775.5:c.*13+221C=	ENSP00000371194.1:n.*13+221C=
ENST00000405957.6:c.*13+221C=	ENSP00000383932.2:n.*13+221C=
ENST00000406638.6:c.*13+221C=	ENSP00000384022.2:n.*13+221C=
ENST00000485341.5:n.1529+221C=
ENST00000612798.4:c.*13+221C=	ENSP00000484140.1:n.*13+221C=
NM_001013253.1:c.*13+221C=	NP_001013271.1:n.*13+221C=
NM_001013254.1:c.*13+221C=	NP_001013272.1:n.*13+221C=
NM_001013255.1:c.*13+221C=	NP_001013273.1:n.*13+221C=
NM_001242932.1:c.*13+221C=	NP_001229861.1:n.*13+221C=
NM_001289005.1:c.*13+221C=	NP_001275934.1:n.*13+221C=
NM_002339.2:c.*13+221C=	NP_002330.1:n.*13+221C=
NM_001013253.2:c.*13+221C=	NP_001013271.1:n.*13+221C=
NM_002339.3:c.*13+221C= MANE Select	NP_002330.1:n.*13+221C=
NM_001242932.2:c.*13+221C=	NP_001229861.1:n.*13+221C=
NM_001289005.2:c.*13+221C=	NP_001275934.1:n.*13+221C=