Canonical Allele Identifier: CA471993616

Gene: LSP1

Linked Data

• MyVariant Identifiers: chr11:g.1908784G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1887554G>T , CM000673.2:g.1887554G>T	GRCh38
NC_000011.9:g.1908784G>T , CM000673.1:g.1908784G>T	GRCh37
NC_000011.8:g.1865360G>T	NCBI36
NG_011509.1:g.39585G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311604.8:c.1011G>T MANE Select	ENSP00000308383.4:p.Pro337=
ENST00000311604.7:c.1011G>T	ENSP00000308383.3:p.Pro337=
ENST00000381775.5:c.1395G>T	ENSP00000371194.1:p.Pro465=
ENST00000405957.6:c.825G>T	ENSP00000383932.2:p.Pro275=
ENST00000406638.6:c.825G>T	ENSP00000384022.2:p.Pro275=
ENST00000472974.5:n.881G>T
ENST00000485341.5:n.1507G>T
ENST00000612798.4:c.825G>T	ENSP00000484140.1:p.Pro275=
NM_001013253.1:c.825G>T	NP_001013271.1:p.Pro275=
NM_001013254.1:c.825G>T	NP_001013272.1:p.Pro275=
NM_001013255.1:c.825G>T	NP_001013273.1:p.Pro275=
NM_001242932.1:c.1395G>T	NP_001229861.1:p.Pro465=
NM_001289005.1:c.825G>T	NP_001275934.1:p.Pro275=
NM_002339.2:c.1011G>T	NP_002330.1:p.Pro337=
NM_001013253.2:c.825G>T	NP_001013271.1:p.Pro275=
NM_002339.3:c.1011G>T MANE Select	NP_002330.1:p.Pro337=
NM_001242932.2:c.1395G>T	NP_001229861.1:p.Pro465=
NM_001289005.2:c.825G>T	NP_001275934.1:p.Pro275=