Canonical Allele Identifier: CA1947897037

Gene: LSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887447T= , CM000673.2:g.1887447T=	GRCh38
NC_000011.9:g.1908677T= , CM000673.1:g.1908677T=	GRCh37
NC_000011.8:g.1865253T=	NCBI36
NG_011509.1:g.39478T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.931-27T= MANE Select	ENSP00000308383.4:n.931-27T=
ENST00000311604.7:c.931-27T=	ENSP00000308383.3:n.931-27T=
ENST00000381775.5:c.1315-27T=	ENSP00000371194.1:n.1315-27T=
ENST00000405957.6:c.745-27T=	ENSP00000383932.2:n.745-27T=
ENST00000406638.6:c.745-27T=	ENSP00000384022.2:n.745-27T=
ENST00000472974.5:n.801-27T=
ENST00000484895.5:n.408-27T=
ENST00000485341.5:n.1427-27T=
ENST00000612798.4:c.745-27T=	ENSP00000484140.1:n.745-27T=
NM_001013253.1:c.745-27T=	NP_001013271.1:n.745-27T=
NM_001013254.1:c.745-27T=	NP_001013272.1:n.745-27T=
NM_001013255.1:c.745-27T=	NP_001013273.1:n.745-27T=
NM_001242932.1:c.1315-27T=	NP_001229861.1:n.1315-27T=
NM_001289005.1:c.745-27T=	NP_001275934.1:n.745-27T=
NM_002339.2:c.931-27T=	NP_002330.1:n.931-27T=
NM_001013253.2:c.745-27T=	NP_001013271.1:n.745-27T=
NM_002339.3:c.931-27T= MANE Select	NP_002330.1:n.931-27T=
NM_001242932.2:c.1315-27T=	NP_001229861.1:n.1315-27T=
NM_001289005.2:c.745-27T=	NP_001275934.1:n.745-27T=