Canonical Allele Identifier: CA216220498

Gene: LSP1

Linked Data

• dbSNP Id: rs374405672
• MyVariant Identifiers: chr11:g.1908994A>G (hg19) ; chr11:g.1887764A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887764A>G , CM000673.2:g.1887764A>G	GRCh38
NC_000011.9:g.1908994A>G , CM000673.1:g.1908994A>G	GRCh37
NC_000011.8:g.1865570A>G	NCBI36
NG_011509.1:g.39795A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000311604.8:c.*13+188A>G MANE Select	ENSP00000308383.4:n.*13+188A>G
ENST00000311604.7:c.*13+188A>G	ENSP00000308383.3:n.*13+188A>G
ENST00000381775.5:c.*13+188A>G	ENSP00000371194.1:n.*13+188A>G
ENST00000405957.6:c.*13+188A>G	ENSP00000383932.2:n.*13+188A>G
ENST00000406638.6:c.*13+188A>G	ENSP00000384022.2:n.*13+188A>G
ENST00000485341.5:n.1529+188A>G
ENST00000612798.4:c.*13+188A>G	ENSP00000484140.1:n.*13+188A>G
NM_001013253.1:c.*13+188A>G	NP_001013271.1:n.*13+188A>G
NM_001013254.1:c.*13+188A>G	NP_001013272.1:n.*13+188A>G
NM_001013255.1:c.*13+188A>G	NP_001013273.1:n.*13+188A>G
NM_001242932.1:c.*13+188A>G	NP_001229861.1:n.*13+188A>G
NM_001289005.1:c.*13+188A>G	NP_001275934.1:n.*13+188A>G
NM_002339.2:c.*13+188A>G	NP_002330.1:n.*13+188A>G
NM_001013253.2:c.*13+188A>G	NP_001013271.1:n.*13+188A>G
NM_002339.3:c.*13+188A>G MANE Select	NP_002330.1:n.*13+188A>G
NM_001242932.2:c.*13+188A>G	NP_001229861.1:n.*13+188A>G
NM_001289005.2:c.*13+188A>G	NP_001275934.1:n.*13+188A>G