Canonical Allele Identifier: CA374938295

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263382A>T (hg19) ; chr9:g.127501103A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501103A>T , CM000671.2:g.127501103A>T	GRCh38
NC_000009.11:g.130263382A>T , CM000671.1:g.130263382A>T	GRCh37
NC_000009.10:g.129303203A>T	NCBI36
NG_032008.1:g.54618A>T , LRG_373:g.54618A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2006A>T MANE Select	ENSP00000300417.6:p.Glu669Val
ENST00000472068.2:c.*1730A>T	ENSP00000501555.1:n.*1730A>T
ENST00000483302.6:n.2671A>T
ENST00000498513.6:c.*897A>T	ENSP00000501637.1:n.*897A>T
ENST00000674511.1:n.1605A>T
ENST00000674516.1:c.*622A>T	ENSP00000502441.1:n.*622A>T
ENST00000674621.1:n.1861-2270A>T
ENST00000674771.1:c.*649A>T	ENSP00000502627.1:n.*649A>T
ENST00000674784.1:c.*1066A>T	ENSP00000501837.1:n.*1066A>T
ENST00000674970.1:c.*1780A>T	ENSP00000502493.1:n.*1780A>T
ENST00000675012.1:n.1950A>T
ENST00000675141.1:c.1907A>T	ENSP00000502420.1:p.Glu636Val
ENST00000675198.1:n.1886A>T
ENST00000675213.1:c.1961A>T	ENSP00000502218.1:p.Glu654Val
ENST00000675224.1:c.*72A>T	ENSP00000501869.1:n.*72A>T
ENST00000675253.1:c.*678A>T	ENSP00000502557.1:n.*678A>T
ENST00000675445.1:c.*1678A>T	ENSP00000502253.1:n.*1678A>T
ENST00000675448.1:c.2006A>T	ENSP00000502167.1:p.Glu669Val
ENST00000675521.1:n.1916A>T
ENST00000675572.1:c.1907A>T	ENSP00000501598.1:p.Glu636Val
ENST00000675641.1:c.*748A>T	ENSP00000501845.1:n.*748A>T
ENST00000675657.1:c.*619A>T	ENSP00000502002.1:n.*619A>T
ENST00000675662.1:n.1801A>T
ENST00000675789.1:c.1826A>T	ENSP00000501954.1:p.Glu609Val
ENST00000675883.1:c.1925A>T	ENSP00000501592.1:p.Glu642Val
ENST00000675945.1:c.*647A>T	ENSP00000501835.1:n.*647A>T
ENST00000676014.1:c.1949A>T	ENSP00000502058.1:p.Glu650Val
ENST00000676035.1:n.1668A>T
ENST00000676106.1:n.2043A>T
ENST00000676137.1:n.2036A>T
ENST00000676170.1:c.2087A>T	ENSP00000502177.1:p.Glu696Val
ENST00000676318.1:c.*2836A>T	ENSP00000502300.1:n.*2836A>T
ENST00000676336.1:c.*619A>T	ENSP00000502686.1:n.*619A>T
ENST00000676349.1:c.*1694A>T	ENSP00000502155.1:n.*1694A>T
ENST00000676399.1:n.1909A>T
ENST00000676409.1:n.2066A>T
ENST00000300417.10:c.2006A>T	ENSP00000300417.6:p.Glu669Val
ENST00000323301.8:c.2006A>T	ENSP00000322937.4:p.Glu669Val
ENST00000373322.1:c.2006A>T	ENSP00000362419.1:p.Glu669Val
ENST00000373324.8:c.1925A>T	ENSP00000362421.4:p.Glu642Val
ENST00000483302.5:n.1228A>T
NM_001005373.3:c.2006A>T	NP_001005373.1:p.Glu669Val
NM_001005374.3:c.2006A>T	NP_001005374.1:p.Glu669Val
NM_001190723.2:c.1925A>T	NP_001177652.1:p.Glu642Val
NM_138361.5:c.2006A>T , LRG_373t1:c.2006A>T	NP_612370.3:p.Glu669Val
XM_006717316.2:c.1907A>T	XP_006717379.1:p.Glu636Val
XM_006717316.4:c.1907A>T	XP_006717379.1:p.Glu636Val
XM_017015283.1:c.2006A>T	XP_016870772.1:p.Glu669Val
XM_017015284.2:c.1217A>T	XP_016870773.1:p.Glu406Val
XR_001746415.2:n.2541A>T
XR_929874.3:n.2365A>T
NM_001190723.3:c.1925A>T	NP_001177652.1:p.Glu642Val
NM_001005373.4:c.2006A>T MANE Select	NP_001005373.1:p.Glu669Val
NM_001005374.4:c.2006A>T	NP_001005374.1:p.Glu669Val
NM_001384142.1:c.2006A>T	NP_001371071.1:p.Glu669Val
NM_001384143.1:c.1907A>T	NP_001371072.1:p.Glu636Val
NM_001384144.1:c.1217A>T	NP_001371073.1:p.Glu406Val
NR_168891.1:n.2535A>T
NR_168892.1:n.2359A>T