Canonical Allele Identifier: CA1879828656
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501072G= , CM000671.2:g.127501072G= GRCh38
NC_000009.11:g.130263351G= , CM000671.1:g.130263351G= GRCh37
NC_000009.10:g.129303172G= NCBI36
NG_032008.1:g.54587G= , LRG_373:g.54587G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1975G= MANE Select ENSP00000300417.6:p.Val659=
ENST00000472068.2:c.*1699G= ENSP00000501555.1:n.*1699G=
ENST00000483302.6:n.2640G=
ENST00000498513.6:c.*866G= ENSP00000501637.1:n.*866G=
ENST00000674511.1:n.1574G=
ENST00000674516.1:c.*591G= ENSP00000502441.1:n.*591G=
ENST00000674621.1:n.1861-2301G=
ENST00000674771.1:c.*618G= ENSP00000502627.1:n.*618G=
ENST00000674784.1:c.*1035G= ENSP00000501837.1:n.*1035G=
ENST00000674970.1:c.*1749G= ENSP00000502493.1:n.*1749G=
ENST00000675012.1:n.1919G=
ENST00000675141.1:c.1876G= ENSP00000502420.1:p.Val626=
ENST00000675198.1:n.1855G=
ENST00000675213.1:c.1930G= ENSP00000502218.1:p.Val644=
ENST00000675224.1:c.*41G= ENSP00000501869.1:n.*41G=
ENST00000675253.1:c.*647G= ENSP00000502557.1:n.*647G=
ENST00000675445.1:c.*1647G= ENSP00000502253.1:n.*1647G=
ENST00000675448.1:c.1975G= ENSP00000502167.1:p.Val659=
ENST00000675521.1:n.1885G=
ENST00000675572.1:c.1876G= ENSP00000501598.1:p.Val626=
ENST00000675641.1:c.*717G= ENSP00000501845.1:n.*717G=
ENST00000675657.1:c.*588G= ENSP00000502002.1:n.*588G=
ENST00000675662.1:n.1770G=
ENST00000675789.1:c.1795G= ENSP00000501954.1:p.Val599=
ENST00000675883.1:c.1894G= ENSP00000501592.1:p.Val632=
ENST00000675945.1:c.*616G= ENSP00000501835.1:n.*616G=
ENST00000676014.1:c.1918G= ENSP00000502058.1:p.Val640=
ENST00000676035.1:n.1637G=
ENST00000676106.1:n.2012G=
ENST00000676137.1:n.2005G=
ENST00000676170.1:c.2056G= ENSP00000502177.1:p.Val686=
ENST00000676318.1:c.*2805G= ENSP00000502300.1:n.*2805G=
ENST00000676336.1:c.*588G= ENSP00000502686.1:n.*588G=
ENST00000676349.1:c.*1663G= ENSP00000502155.1:n.*1663G=
ENST00000676399.1:n.1878G=
ENST00000676409.1:n.2035G=
ENST00000300417.10:c.1975G= ENSP00000300417.6:p.Val659=
ENST00000323301.8:c.1975G= ENSP00000322937.4:p.Val659=
ENST00000373322.1:c.1975G= ENSP00000362419.1:p.Val659=
ENST00000373324.8:c.1894G= ENSP00000362421.4:p.Val632=
ENST00000483302.5:n.1197G=
NM_001005373.3:c.1975G= NP_001005373.1:p.Val659=
NM_001005374.3:c.1975G= NP_001005374.1:p.Val659=
NM_001190723.2:c.1894G= NP_001177652.1:p.Val632=
NM_138361.5:c.1975G= , LRG_373t1:c.1975G= NP_612370.3:p.Val659=
XM_006717316.2:c.1876G= XP_006717379.1:p.Val626=
XM_006717316.4:c.1876G= XP_006717379.1:p.Val626=
XM_017015283.1:c.1975G= XP_016870772.1:p.Val659=
XM_017015284.2:c.1186G= XP_016870773.1:p.Val396=
XR_001746415.2:n.2510G=
XR_929874.3:n.2334G=
NM_001190723.3:c.1894G= NP_001177652.1:p.Val632=
NM_001005373.4:c.1975G= MANE Select NP_001005373.1:p.Val659=
NM_001005374.4:c.1975G= NP_001005374.1:p.Val659=
NM_001384142.1:c.1975G= NP_001371071.1:p.Val659=
NM_001384143.1:c.1876G= NP_001371072.1:p.Val626=
NM_001384144.1:c.1186G= NP_001371073.1:p.Val396=
NR_168891.1:n.2504G=
NR_168892.1:n.2328G=