Canonical Allele Identifier: CA2611944001
Gene: LSP1 HGNC NCBI

Linked Data

gnomAD v4: 11-1887471-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1887471C>A , CM000673.2:g.1887471C>A GRCh38
NC_000011.9:g.1908701C>A , CM000673.1:g.1908701C>A GRCh37
NC_000011.8:g.1865277C>A NCBI36
NG_011509.1:g.39502C>A

Transcript Alleles

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