Canonical Allele Identifier: CA2574787578

Gene: LSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887572T>C , CM000673.2:g.1887572T>C	GRCh38
NC_000011.9:g.1908802T>C , CM000673.1:g.1908802T>C	GRCh37
NC_000011.8:g.1865378T>C	NCBI36
NG_011509.1:g.39603T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.*9T>C MANE Select	ENSP00000308383.4:n.*9T>C
ENST00000311604.7:c.*9T>C	ENSP00000308383.3:n.*9T>C
ENST00000381775.5:c.*9T>C	ENSP00000371194.1:n.*9T>C
ENST00000405957.6:c.*9T>C	ENSP00000383932.2:n.*9T>C
ENST00000406638.6:c.*9T>C	ENSP00000384022.2:n.*9T>C
ENST00000472974.5:n.899T>C
ENST00000485341.5:n.1525T>C
ENST00000612798.4:c.*9T>C	ENSP00000484140.1:n.*9T>C
NM_001013253.1:c.*9T>C	NP_001013271.1:n.*9T>C
NM_001013254.1:c.*9T>C	NP_001013272.1:n.*9T>C
NM_001013255.1:c.*9T>C	NP_001013273.1:n.*9T>C
NM_001242932.1:c.*9T>C	NP_001229861.1:n.*9T>C
NM_001289005.1:c.*9T>C	NP_001275934.1:n.*9T>C
NM_002339.2:c.*9T>C	NP_002330.1:n.*9T>C
NM_001013253.2:c.*9T>C	NP_001013271.1:n.*9T>C
NM_002339.3:c.*9T>C MANE Select	NP_002330.1:n.*9T>C
NM_001242932.2:c.*9T>C	NP_001229861.1:n.*9T>C
NM_001289005.2:c.*9T>C	NP_001275934.1:n.*9T>C