Canonical Allele Identifier: CA467236770

Gene: LRSAM1

Linked Data

• dbSNP Id: rs1190478414
• gnomAD v2: 9-130263353-G-A
• MyVariant Identifiers: chr9:g.130263353G>A (hg19) ; chr9:g.127501074G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501074G>A , CM000671.2:g.127501074G>A	GRCh38
NC_000009.11:g.130263353G>A , CM000671.1:g.130263353G>A	GRCh37
NC_000009.10:g.129303174G>A	NCBI36
NG_032008.1:g.54589G>A , LRG_373:g.54589G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1977G>A MANE Select	ENSP00000300417.6:p.Val659=
ENST00000472068.2:c.*1701G>A	ENSP00000501555.1:n.*1701G>A
ENST00000483302.6:n.2642G>A
ENST00000498513.6:c.*868G>A	ENSP00000501637.1:n.*868G>A
ENST00000674511.1:n.1576G>A
ENST00000674516.1:c.*593G>A	ENSP00000502441.1:n.*593G>A
ENST00000674621.1:n.1861-2299G>A
ENST00000674771.1:c.*620G>A	ENSP00000502627.1:n.*620G>A
ENST00000674784.1:c.*1037G>A	ENSP00000501837.1:n.*1037G>A
ENST00000674970.1:c.*1751G>A	ENSP00000502493.1:n.*1751G>A
ENST00000675012.1:n.1921G>A
ENST00000675141.1:c.1878G>A	ENSP00000502420.1:p.Val626=
ENST00000675198.1:n.1857G>A
ENST00000675213.1:c.1932G>A	ENSP00000502218.1:p.Val644=
ENST00000675224.1:c.*43G>A	ENSP00000501869.1:n.*43G>A
ENST00000675253.1:c.*649G>A	ENSP00000502557.1:n.*649G>A
ENST00000675445.1:c.*1649G>A	ENSP00000502253.1:n.*1649G>A
ENST00000675448.1:c.1977G>A	ENSP00000502167.1:p.Val659=
ENST00000675521.1:n.1887G>A
ENST00000675572.1:c.1878G>A	ENSP00000501598.1:p.Val626=
ENST00000675641.1:c.*719G>A	ENSP00000501845.1:n.*719G>A
ENST00000675657.1:c.*590G>A	ENSP00000502002.1:n.*590G>A
ENST00000675662.1:n.1772G>A
ENST00000675789.1:c.1797G>A	ENSP00000501954.1:p.Val599=
ENST00000675883.1:c.1896G>A	ENSP00000501592.1:p.Val632=
ENST00000675945.1:c.*618G>A	ENSP00000501835.1:n.*618G>A
ENST00000676014.1:c.1920G>A	ENSP00000502058.1:p.Val640=
ENST00000676035.1:n.1639G>A
ENST00000676106.1:n.2014G>A
ENST00000676137.1:n.2007G>A
ENST00000676170.1:c.2058G>A	ENSP00000502177.1:p.Val686=
ENST00000676318.1:c.*2807G>A	ENSP00000502300.1:n.*2807G>A
ENST00000676336.1:c.*590G>A	ENSP00000502686.1:n.*590G>A
ENST00000676349.1:c.*1665G>A	ENSP00000502155.1:n.*1665G>A
ENST00000676399.1:n.1880G>A
ENST00000676409.1:n.2037G>A
ENST00000300417.10:c.1977G>A	ENSP00000300417.6:p.Val659=
ENST00000323301.8:c.1977G>A	ENSP00000322937.4:p.Val659=
ENST00000373322.1:c.1977G>A	ENSP00000362419.1:p.Val659=
ENST00000373324.8:c.1896G>A	ENSP00000362421.4:p.Val632=
ENST00000483302.5:n.1199G>A
NM_001005373.3:c.1977G>A	NP_001005373.1:p.Val659=
NM_001005374.3:c.1977G>A	NP_001005374.1:p.Val659=
NM_001190723.2:c.1896G>A	NP_001177652.1:p.Val632=
NM_138361.5:c.1977G>A , LRG_373t1:c.1977G>A	NP_612370.3:p.Val659=
XM_006717316.2:c.1878G>A	XP_006717379.1:p.Val626=
XM_006717316.4:c.1878G>A	XP_006717379.1:p.Val626=
XM_017015283.1:c.1977G>A	XP_016870772.1:p.Val659=
XM_017015284.2:c.1188G>A	XP_016870773.1:p.Val396=
XR_001746415.2:n.2512G>A
XR_929874.3:n.2336G>A
NM_001190723.3:c.1896G>A	NP_001177652.1:p.Val632=
NM_001005373.4:c.1977G>A MANE Select	NP_001005373.1:p.Val659=
NM_001005374.4:c.1977G>A	NP_001005374.1:p.Val659=
NM_001384142.1:c.1977G>A	NP_001371071.1:p.Val659=
NM_001384143.1:c.1878G>A	NP_001371072.1:p.Val626=
NM_001384144.1:c.1188G>A	NP_001371073.1:p.Val396=
NR_168891.1:n.2506G>A
NR_168892.1:n.2330G>A