Canonical Allele Identifier: CA1879828678
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501080A= , CM000671.2:g.127501080A= GRCh38
NC_000009.11:g.130263359A= , CM000671.1:g.130263359A= GRCh37
NC_000009.10:g.129303180A= NCBI36
NG_032008.1:g.54595A= , LRG_373:g.54595A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1983A= MANE Select ENSP00000300417.6:p.Pro661=
ENST00000472068.2:c.*1707A= ENSP00000501555.1:n.*1707A=
ENST00000483302.6:n.2648A=
ENST00000498513.6:c.*874A= ENSP00000501637.1:n.*874A=
ENST00000674511.1:n.1582A=
ENST00000674516.1:c.*599A= ENSP00000502441.1:n.*599A=
ENST00000674621.1:n.1861-2293A=
ENST00000674771.1:c.*626A= ENSP00000502627.1:n.*626A=
ENST00000674784.1:c.*1043A= ENSP00000501837.1:n.*1043A=
ENST00000674970.1:c.*1757A= ENSP00000502493.1:n.*1757A=
ENST00000675012.1:n.1927A=
ENST00000675141.1:c.1884A= ENSP00000502420.1:p.Pro628=
ENST00000675198.1:n.1863A=
ENST00000675213.1:c.1938A= ENSP00000502218.1:p.Pro646=
ENST00000675224.1:c.*49A= ENSP00000501869.1:n.*49A=
ENST00000675253.1:c.*655A= ENSP00000502557.1:n.*655A=
ENST00000675445.1:c.*1655A= ENSP00000502253.1:n.*1655A=
ENST00000675448.1:c.1983A= ENSP00000502167.1:p.Pro661=
ENST00000675521.1:n.1893A=
ENST00000675572.1:c.1884A= ENSP00000501598.1:p.Pro628=
ENST00000675641.1:c.*725A= ENSP00000501845.1:n.*725A=
ENST00000675657.1:c.*596A= ENSP00000502002.1:n.*596A=
ENST00000675662.1:n.1778A=
ENST00000675789.1:c.1803A= ENSP00000501954.1:p.Pro601=
ENST00000675883.1:c.1902A= ENSP00000501592.1:p.Pro634=
ENST00000675945.1:c.*624A= ENSP00000501835.1:n.*624A=
ENST00000676014.1:c.1926A= ENSP00000502058.1:p.Pro642=
ENST00000676035.1:n.1645A=
ENST00000676106.1:n.2020A=
ENST00000676137.1:n.2013A=
ENST00000676170.1:c.2064A= ENSP00000502177.1:p.Pro688=
ENST00000676318.1:c.*2813A= ENSP00000502300.1:n.*2813A=
ENST00000676336.1:c.*596A= ENSP00000502686.1:n.*596A=
ENST00000676349.1:c.*1671A= ENSP00000502155.1:n.*1671A=
ENST00000676399.1:n.1886A=
ENST00000676409.1:n.2043A=
ENST00000300417.10:c.1983A= ENSP00000300417.6:p.Pro661=
ENST00000323301.8:c.1983A= ENSP00000322937.4:p.Pro661=
ENST00000373322.1:c.1983A= ENSP00000362419.1:p.Pro661=
ENST00000373324.8:c.1902A= ENSP00000362421.4:p.Pro634=
ENST00000483302.5:n.1205A=
NM_001005373.3:c.1983A= NP_001005373.1:p.Pro661=
NM_001005374.3:c.1983A= NP_001005374.1:p.Pro661=
NM_001190723.2:c.1902A= NP_001177652.1:p.Pro634=
NM_138361.5:c.1983A= , LRG_373t1:c.1983A= NP_612370.3:p.Pro661=
XM_006717316.2:c.1884A= XP_006717379.1:p.Pro628=
XM_006717316.4:c.1884A= XP_006717379.1:p.Pro628=
XM_017015283.1:c.1983A= XP_016870772.1:p.Pro661=
XM_017015284.2:c.1194A= XP_016870773.1:p.Pro398=
XR_001746415.2:n.2518A=
XR_929874.3:n.2342A=
NM_001190723.3:c.1902A= NP_001177652.1:p.Pro634=
NM_001005373.4:c.1983A= MANE Select NP_001005373.1:p.Pro661=
NM_001005374.4:c.1983A= NP_001005374.1:p.Pro661=
NM_001384142.1:c.1983A= NP_001371071.1:p.Pro661=
NM_001384143.1:c.1884A= NP_001371072.1:p.Pro628=
NM_001384144.1:c.1194A= NP_001371073.1:p.Pro398=
NR_168891.1:n.2512A=
NR_168892.1:n.2336A=