Canonical Allele Identifier: CA1879828503
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501028G= , CM000671.2:g.127501028G= GRCh38
NC_000009.11:g.130263307G= , CM000671.1:g.130263307G= GRCh37
NC_000009.10:g.129303128G= NCBI36
NG_032008.1:g.54543G= , LRG_373:g.54543G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1931G= MANE Select ENSP00000300417.6:p.Gly644=
ENST00000472068.2:c.*1655G= ENSP00000501555.1:n.*1655G=
ENST00000483302.6:n.2596G=
ENST00000498513.6:c.*822G= ENSP00000501637.1:n.*822G=
ENST00000674511.1:n.1530G=
ENST00000674516.1:c.*547G= ENSP00000502441.1:n.*547G=
ENST00000674621.1:n.1861-2345G=
ENST00000674771.1:c.*574G= ENSP00000502627.1:n.*574G=
ENST00000674784.1:c.*991G= ENSP00000501837.1:n.*991G=
ENST00000674970.1:c.*1705G= ENSP00000502493.1:n.*1705G=
ENST00000675012.1:n.1875G=
ENST00000675141.1:c.1832G= ENSP00000502420.1:p.Gly611=
ENST00000675198.1:n.1811G=
ENST00000675213.1:c.1886G= ENSP00000502218.1:p.Gly629=
ENST00000675224.1:c.1959G= ENSP00000501869.1:p.Gly653=
ENST00000675253.1:c.*603G= ENSP00000502557.1:n.*603G=
ENST00000675445.1:c.*1603G= ENSP00000502253.1:n.*1603G=
ENST00000675448.1:c.1931G= ENSP00000502167.1:p.Gly644=
ENST00000675521.1:n.1841G=
ENST00000675572.1:c.1832G= ENSP00000501598.1:p.Gly611=
ENST00000675641.1:c.*673G= ENSP00000501845.1:n.*673G=
ENST00000675657.1:c.*544G= ENSP00000502002.1:n.*544G=
ENST00000675662.1:n.1726G=
ENST00000675789.1:c.1751G= ENSP00000501954.1:p.Gly584=
ENST00000675883.1:c.1850G= ENSP00000501592.1:p.Gly617=
ENST00000675945.1:c.*572G= ENSP00000501835.1:n.*572G=
ENST00000676014.1:c.1874G= ENSP00000502058.1:p.Gly625=
ENST00000676035.1:n.1593G=
ENST00000676106.1:n.1968G=
ENST00000676137.1:n.1961G=
ENST00000676170.1:c.2012G= ENSP00000502177.1:p.Gly671=
ENST00000676318.1:c.*2761G= ENSP00000502300.1:n.*2761G=
ENST00000676336.1:c.*544G= ENSP00000502686.1:n.*544G=
ENST00000676349.1:c.*1619G= ENSP00000502155.1:n.*1619G=
ENST00000676399.1:n.1834G=
ENST00000676409.1:n.1991G=
ENST00000300417.10:c.1931G= ENSP00000300417.6:p.Gly644=
ENST00000323301.8:c.1931G= ENSP00000322937.4:p.Gly644=
ENST00000373322.1:c.1931G= ENSP00000362419.1:p.Gly644=
ENST00000373324.8:c.1850G= ENSP00000362421.4:p.Gly617=
ENST00000472068.1:n.824G=
ENST00000483302.5:n.1153G=
NM_001005373.3:c.1931G= NP_001005373.1:p.Gly644=
NM_001005374.3:c.1931G= NP_001005374.1:p.Gly644=
NM_001190723.2:c.1850G= NP_001177652.1:p.Gly617=
NM_138361.5:c.1931G= , LRG_373t1:c.1931G= NP_612370.3:p.Gly644=
XM_006717316.2:c.1832G= XP_006717379.1:p.Gly611=
XM_006717316.4:c.1832G= XP_006717379.1:p.Gly611=
XM_017015283.1:c.1931G= XP_016870772.1:p.Gly644=
XM_017015284.2:c.1142G= XP_016870773.1:p.Gly381=
XR_001746415.2:n.2466G=
XR_929874.3:n.2290G=
NM_001190723.3:c.1850G= NP_001177652.1:p.Gly617=
NM_001005373.4:c.1931G= MANE Select NP_001005373.1:p.Gly644=
NM_001005374.4:c.1931G= NP_001005374.1:p.Gly644=
NM_001384142.1:c.1931G= NP_001371071.1:p.Gly644=
NM_001384143.1:c.1832G= NP_001371072.1:p.Gly611=
NM_001384144.1:c.1142G= NP_001371073.1:p.Gly381=
NR_168891.1:n.2460G=
NR_168892.1:n.2284G=