Canonical Allele Identifier: CA216220506

Gene: LSP1

Linked Data

• dbSNP Id: rs562333167
• gnomAD v2: 11-1908997-C-A
• gnomAD v3: 11-1887767-C-A
• gnomAD v4: 11-1887767-C-A
• MyVariant Identifiers: chr11:g.1908997C>A (hg19) ; chr11:g.1887767C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887767C>A , CM000673.2:g.1887767C>A	GRCh38
NC_000011.9:g.1908997C>A , CM000673.1:g.1908997C>A	GRCh37
NC_000011.8:g.1865573C>A	NCBI36
NG_011509.1:g.39798C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000311604.8:c.*13+191C>A MANE Select	ENSP00000308383.4:n.*13+191C>A
ENST00000311604.7:c.*13+191C>A	ENSP00000308383.3:n.*13+191C>A
ENST00000381775.5:c.*13+191C>A	ENSP00000371194.1:n.*13+191C>A
ENST00000405957.6:c.*13+191C>A	ENSP00000383932.2:n.*13+191C>A
ENST00000406638.6:c.*13+191C>A	ENSP00000384022.2:n.*13+191C>A
ENST00000485341.5:n.1529+191C>A
ENST00000612798.4:c.*13+191C>A	ENSP00000484140.1:n.*13+191C>A
NM_001013253.1:c.*13+191C>A	NP_001013271.1:n.*13+191C>A
NM_001013254.1:c.*13+191C>A	NP_001013272.1:n.*13+191C>A
NM_001013255.1:c.*13+191C>A	NP_001013273.1:n.*13+191C>A
NM_001242932.1:c.*13+191C>A	NP_001229861.1:n.*13+191C>A
NM_001289005.1:c.*13+191C>A	NP_001275934.1:n.*13+191C>A
NM_002339.2:c.*13+191C>A	NP_002330.1:n.*13+191C>A
NM_001013253.2:c.*13+191C>A	NP_001013271.1:n.*13+191C>A
NM_002339.3:c.*13+191C>A MANE Select	NP_002330.1:n.*13+191C>A
NM_001242932.2:c.*13+191C>A	NP_001229861.1:n.*13+191C>A
NM_001289005.2:c.*13+191C>A	NP_001275934.1:n.*13+191C>A