Canonical Allele Identifier: CA1947897064

Gene: LSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887505T= , CM000673.2:g.1887505T=	GRCh38
NC_000011.9:g.1908735T= , CM000673.1:g.1908735T=	GRCh37
NC_000011.8:g.1865311T=	NCBI36
NG_011509.1:g.39536T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.962T= MANE Select	ENSP00000308383.4:p.Val321=
ENST00000311604.7:c.962T=	ENSP00000308383.3:p.Val321=
ENST00000381775.5:c.1346T=	ENSP00000371194.1:p.Val449=
ENST00000405957.6:c.776T=	ENSP00000383932.2:p.Val259=
ENST00000406638.6:c.776T=	ENSP00000384022.2:p.Val259=
ENST00000472974.5:n.832T=
ENST00000485341.5:n.1458T=
ENST00000612798.4:c.776T=	ENSP00000484140.1:p.Val259=
NM_001013253.1:c.776T=	NP_001013271.1:p.Val259=
NM_001013254.1:c.776T=	NP_001013272.1:p.Val259=
NM_001013255.1:c.776T=	NP_001013273.1:p.Val259=
NM_001242932.1:c.1346T=	NP_001229861.1:p.Val449=
NM_001289005.1:c.776T=	NP_001275934.1:p.Val259=
NM_002339.2:c.962T=	NP_002330.1:p.Val321=
NM_001013253.2:c.776T=	NP_001013271.1:p.Val259=
NM_002339.3:c.962T= MANE Select	NP_002330.1:p.Val321=
NM_001242932.2:c.1346T=	NP_001229861.1:p.Val449=
NM_001289005.2:c.776T=	NP_001275934.1:p.Val259=