Canonical Allele Identifier: CA1879828475
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501021C= , CM000671.2:g.127501021C= GRCh38
NC_000009.11:g.130263300C= , CM000671.1:g.130263300C= GRCh37
NC_000009.10:g.129303121C= NCBI36
NG_032008.1:g.54536C= , LRG_373:g.54536C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1924C= MANE Select ENSP00000300417.6:p.Pro642=
ENST00000472068.2:c.*1648C= ENSP00000501555.1:n.*1648C=
ENST00000483302.6:n.2589C=
ENST00000498513.6:c.*815C= ENSP00000501637.1:n.*815C=
ENST00000674511.1:n.1523C=
ENST00000674516.1:c.*540C= ENSP00000502441.1:n.*540C=
ENST00000674621.1:n.1861-2352C=
ENST00000674771.1:c.*567C= ENSP00000502627.1:n.*567C=
ENST00000674784.1:c.*984C= ENSP00000501837.1:n.*984C=
ENST00000674970.1:c.*1698C= ENSP00000502493.1:n.*1698C=
ENST00000675012.1:n.1868C=
ENST00000675141.1:c.1825C= ENSP00000502420.1:p.Pro609=
ENST00000675198.1:n.1804C=
ENST00000675213.1:c.1879C= ENSP00000502218.1:p.Pro627=
ENST00000675224.1:c.1952C= ENSP00000501869.1:p.Thr651=
ENST00000675253.1:c.*596C= ENSP00000502557.1:n.*596C=
ENST00000675445.1:c.*1596C= ENSP00000502253.1:n.*1596C=
ENST00000675448.1:c.1924C= ENSP00000502167.1:p.Pro642=
ENST00000675521.1:n.1834C=
ENST00000675572.1:c.1825C= ENSP00000501598.1:p.Pro609=
ENST00000675641.1:c.*666C= ENSP00000501845.1:n.*666C=
ENST00000675657.1:c.*537C= ENSP00000502002.1:n.*537C=
ENST00000675662.1:n.1719C=
ENST00000675789.1:c.1744C= ENSP00000501954.1:p.Pro582=
ENST00000675883.1:c.1843C= ENSP00000501592.1:p.Pro615=
ENST00000675945.1:c.*565C= ENSP00000501835.1:n.*565C=
ENST00000676014.1:c.1867C= ENSP00000502058.1:p.Pro623=
ENST00000676035.1:n.1586C=
ENST00000676106.1:n.1961C=
ENST00000676137.1:n.1954C=
ENST00000676170.1:c.2005C= ENSP00000502177.1:p.Pro669=
ENST00000676318.1:c.*2754C= ENSP00000502300.1:n.*2754C=
ENST00000676336.1:c.*537C= ENSP00000502686.1:n.*537C=
ENST00000676349.1:c.*1612C= ENSP00000502155.1:n.*1612C=
ENST00000676399.1:n.1827C=
ENST00000676409.1:n.1984C=
ENST00000300417.10:c.1924C= ENSP00000300417.6:p.Pro642=
ENST00000323301.8:c.1924C= ENSP00000322937.4:p.Pro642=
ENST00000373322.1:c.1924C= ENSP00000362419.1:p.Pro642=
ENST00000373324.8:c.1843C= ENSP00000362421.4:p.Pro615=
ENST00000472068.1:n.817C=
ENST00000483302.5:n.1146C=
NM_001005373.3:c.1924C= NP_001005373.1:p.Pro642=
NM_001005374.3:c.1924C= NP_001005374.1:p.Pro642=
NM_001190723.2:c.1843C= NP_001177652.1:p.Pro615=
NM_138361.5:c.1924C= , LRG_373t1:c.1924C= NP_612370.3:p.Pro642=
XM_006717316.2:c.1825C= XP_006717379.1:p.Pro609=
XM_006717316.4:c.1825C= XP_006717379.1:p.Pro609=
XM_017015283.1:c.1924C= XP_016870772.1:p.Pro642=
XM_017015284.2:c.1135C= XP_016870773.1:p.Pro379=
XR_001746415.2:n.2459C=
XR_929874.3:n.2283C=
NM_001190723.3:c.1843C= NP_001177652.1:p.Pro615=
NM_001005373.4:c.1924C= MANE Select NP_001005373.1:p.Pro642=
NM_001005374.4:c.1924C= NP_001005374.1:p.Pro642=
NM_001384142.1:c.1924C= NP_001371071.1:p.Pro642=
NM_001384143.1:c.1825C= NP_001371072.1:p.Pro609=
NM_001384144.1:c.1135C= NP_001371073.1:p.Pro379=
NR_168891.1:n.2453C=
NR_168892.1:n.2277C=