Canonical Allele Identifier: CA1879828752
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501102G= , CM000671.2:g.127501102G= GRCh38
NC_000009.11:g.130263381G= , CM000671.1:g.130263381G= GRCh37
NC_000009.10:g.129303202G= NCBI36
NG_032008.1:g.54617G= , LRG_373:g.54617G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.2005G= MANE Select ENSP00000300417.6:p.Glu669=
ENST00000472068.2:c.*1729G= ENSP00000501555.1:n.*1729G=
ENST00000483302.6:n.2670G=
ENST00000498513.6:c.*896G= ENSP00000501637.1:n.*896G=
ENST00000674511.1:n.1604G=
ENST00000674516.1:c.*621G= ENSP00000502441.1:n.*621G=
ENST00000674621.1:n.1861-2271G=
ENST00000674771.1:c.*648G= ENSP00000502627.1:n.*648G=
ENST00000674784.1:c.*1065G= ENSP00000501837.1:n.*1065G=
ENST00000674970.1:c.*1779G= ENSP00000502493.1:n.*1779G=
ENST00000675012.1:n.1949G=
ENST00000675141.1:c.1906G= ENSP00000502420.1:p.Glu636=
ENST00000675198.1:n.1885G=
ENST00000675213.1:c.1960G= ENSP00000502218.1:p.Glu654=
ENST00000675224.1:c.*71G= ENSP00000501869.1:n.*71G=
ENST00000675253.1:c.*677G= ENSP00000502557.1:n.*677G=
ENST00000675445.1:c.*1677G= ENSP00000502253.1:n.*1677G=
ENST00000675448.1:c.2005G= ENSP00000502167.1:p.Glu669=
ENST00000675521.1:n.1915G=
ENST00000675572.1:c.1906G= ENSP00000501598.1:p.Glu636=
ENST00000675641.1:c.*747G= ENSP00000501845.1:n.*747G=
ENST00000675657.1:c.*618G= ENSP00000502002.1:n.*618G=
ENST00000675662.1:n.1800G=
ENST00000675789.1:c.1825G= ENSP00000501954.1:p.Glu609=
ENST00000675883.1:c.1924G= ENSP00000501592.1:p.Glu642=
ENST00000675945.1:c.*646G= ENSP00000501835.1:n.*646G=
ENST00000676014.1:c.1948G= ENSP00000502058.1:p.Glu650=
ENST00000676035.1:n.1667G=
ENST00000676106.1:n.2042G=
ENST00000676137.1:n.2035G=
ENST00000676170.1:c.2086G= ENSP00000502177.1:p.Glu696=
ENST00000676318.1:c.*2835G= ENSP00000502300.1:n.*2835G=
ENST00000676336.1:c.*618G= ENSP00000502686.1:n.*618G=
ENST00000676349.1:c.*1693G= ENSP00000502155.1:n.*1693G=
ENST00000676399.1:n.1908G=
ENST00000676409.1:n.2065G=
ENST00000300417.10:c.2005G= ENSP00000300417.6:p.Glu669=
ENST00000323301.8:c.2005G= ENSP00000322937.4:p.Glu669=
ENST00000373322.1:c.2005G= ENSP00000362419.1:p.Glu669=
ENST00000373324.8:c.1924G= ENSP00000362421.4:p.Glu642=
ENST00000483302.5:n.1227G=
NM_001005373.3:c.2005G= NP_001005373.1:p.Glu669=
NM_001005374.3:c.2005G= NP_001005374.1:p.Glu669=
NM_001190723.2:c.1924G= NP_001177652.1:p.Glu642=
NM_138361.5:c.2005G= , LRG_373t1:c.2005G= NP_612370.3:p.Glu669=
XM_006717316.2:c.1906G= XP_006717379.1:p.Glu636=
XM_006717316.4:c.1906G= XP_006717379.1:p.Glu636=
XM_017015283.1:c.2005G= XP_016870772.1:p.Glu669=
XM_017015284.2:c.1216G= XP_016870773.1:p.Glu406=
XR_001746415.2:n.2540G=
XR_929874.3:n.2364G=
NM_001190723.3:c.1924G= NP_001177652.1:p.Glu642=
NM_001005373.4:c.2005G= MANE Select NP_001005373.1:p.Glu669=
NM_001005374.4:c.2005G= NP_001005374.1:p.Glu669=
NM_001384142.1:c.2005G= NP_001371071.1:p.Glu669=
NM_001384143.1:c.1906G= NP_001371072.1:p.Glu636=
NM_001384144.1:c.1216G= NP_001371073.1:p.Glu406=
NR_168891.1:n.2534G=
NR_168892.1:n.2358G=