Canonical Allele Identifier: CA2790180572

Gene: LSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887528_1887530del , CM000673.2:g.1887528_1887530del	GRCh38
NC_000011.9:g.1908758_1908760del , CM000673.1:g.1908758_1908760del	GRCh37
NC_000011.8:g.1865334_1865336del	NCBI36
NG_011509.1:g.39559_39561del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.985_987del MANE Select	ENSP00000308383.4:p.Glu329del
ENST00000311604.7:c.985_987del	ENSP00000308383.3:p.Glu329del
ENST00000381775.5:c.1369_1371del	ENSP00000371194.1:p.Glu457del
ENST00000405957.6:c.799_801del	ENSP00000383932.2:p.Glu267del
ENST00000406638.6:c.799_801del	ENSP00000384022.2:p.Glu267del
ENST00000472974.5:n.855_857del
ENST00000485341.5:n.1481_1483del
ENST00000612798.4:c.799_801del	ENSP00000484140.1:p.Glu267del
NM_001013253.1:c.799_801del	NP_001013271.1:p.Glu267del
NM_001013254.1:c.799_801del	NP_001013272.1:p.Glu267del
NM_001013255.1:c.799_801del	NP_001013273.1:p.Glu267del
NM_001242932.1:c.1369_1371del	NP_001229861.1:p.Glu457del
NM_001289005.1:c.799_801del	NP_001275934.1:p.Glu267del
NM_002339.2:c.985_987del	NP_002330.1:p.Glu329del
NM_001013253.2:c.799_801del	NP_001013271.1:p.Glu267del
NM_002339.3:c.985_987del MANE Select	NP_002330.1:p.Glu329del
NM_001242932.2:c.1369_1371del	NP_001229861.1:p.Glu457del
NM_001289005.2:c.799_801del	NP_001275934.1:p.Glu267del