Canonical Allele Identifier: CA216220022

Gene: LSP1

Linked Data

• dbSNP Id: rs879090185
• gnomAD v4: 11-1887426-C-T
• MyVariant Identifiers: chr11:g.1908656C>T (hg19) ; chr11:g.1887426C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887426C>T , CM000673.2:g.1887426C>T	GRCh38
NC_000011.9:g.1908656C>T , CM000673.1:g.1908656C>T	GRCh37
NC_000011.8:g.1865232C>T	NCBI36
NG_011509.1:g.39457C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.931-48C>T MANE Select	ENSP00000308383.4:n.931-48C>T
ENST00000311604.7:c.931-48C>T	ENSP00000308383.3:n.931-48C>T
ENST00000381775.5:c.1315-48C>T	ENSP00000371194.1:n.1315-48C>T
ENST00000405957.6:c.745-48C>T	ENSP00000383932.2:n.745-48C>T
ENST00000406638.6:c.745-48C>T	ENSP00000384022.2:n.745-48C>T
ENST00000472974.5:n.801-48C>T
ENST00000484895.5:n.408-48C>T
ENST00000485341.5:n.1427-48C>T
ENST00000612798.4:c.745-48C>T	ENSP00000484140.1:n.745-48C>T
NM_001013253.1:c.745-48C>T	NP_001013271.1:n.745-48C>T
NM_001013254.1:c.745-48C>T	NP_001013272.1:n.745-48C>T
NM_001013255.1:c.745-48C>T	NP_001013273.1:n.745-48C>T
NM_001242932.1:c.1315-48C>T	NP_001229861.1:n.1315-48C>T
NM_001289005.1:c.745-48C>T	NP_001275934.1:n.745-48C>T
NM_002339.2:c.931-48C>T	NP_002330.1:n.931-48C>T
NM_001013253.2:c.745-48C>T	NP_001013271.1:n.745-48C>T
NM_002339.3:c.931-48C>T MANE Select	NP_002330.1:n.931-48C>T
NM_001242932.2:c.1315-48C>T	NP_001229861.1:n.1315-48C>T
NM_001289005.2:c.745-48C>T	NP_001275934.1:n.745-48C>T