Canonical Allele Identifier: CA379108931
Gene: LSP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1887538T>A , CM000673.2:g.1887538T>A GRCh38
NC_000011.9:g.1908768T>A , CM000673.1:g.1908768T>A GRCh37
NC_000011.8:g.1865344T>A NCBI36
NG_011509.1:g.39569T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311604.8:c.995T>A MANE Select ENSP00000308383.4:p.Leu332His
ENST00000311604.7:c.995T>A ENSP00000308383.3:p.Leu332His
ENST00000381775.5:c.1379T>A ENSP00000371194.1:p.Leu460His
ENST00000405957.6:c.809T>A ENSP00000383932.2:p.Leu270His
ENST00000406638.6:c.809T>A ENSP00000384022.2:p.Leu270His
ENST00000472974.5:n.865T>A
ENST00000485341.5:n.1491T>A
ENST00000612798.4:c.809T>A ENSP00000484140.1:p.Leu270His
NM_001013253.1:c.809T>A NP_001013271.1:p.Leu270His
NM_001013254.1:c.809T>A NP_001013272.1:p.Leu270His
NM_001013255.1:c.809T>A NP_001013273.1:p.Leu270His
NM_001242932.1:c.1379T>A NP_001229861.1:p.Leu460His
NM_001289005.1:c.809T>A NP_001275934.1:p.Leu270His
NM_002339.2:c.995T>A NP_002330.1:p.Leu332His
NM_001013253.2:c.809T>A NP_001013271.1:p.Leu270His
NM_002339.3:c.995T>A MANE Select NP_002330.1:p.Leu332His
NM_001242932.2:c.1379T>A NP_001229861.1:p.Leu460His
NM_001289005.2:c.809T>A NP_001275934.1:p.Leu270His