Canonical Allele Identifier: CA1879828570
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501048G= , CM000671.2:g.127501048G= GRCh38
NC_000009.11:g.130263327G= , CM000671.1:g.130263327G= GRCh37
NC_000009.10:g.129303148G= NCBI36
NG_032008.1:g.54563G= , LRG_373:g.54563G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1951G= MANE Select ENSP00000300417.6:p.Ala651=
ENST00000472068.2:c.*1675G= ENSP00000501555.1:n.*1675G=
ENST00000483302.6:n.2616G=
ENST00000498513.6:c.*842G= ENSP00000501637.1:n.*842G=
ENST00000674511.1:n.1550G=
ENST00000674516.1:c.*567G= ENSP00000502441.1:n.*567G=
ENST00000674621.1:n.1861-2325G=
ENST00000674771.1:c.*594G= ENSP00000502627.1:n.*594G=
ENST00000674784.1:c.*1011G= ENSP00000501837.1:n.*1011G=
ENST00000674970.1:c.*1725G= ENSP00000502493.1:n.*1725G=
ENST00000675012.1:n.1895G=
ENST00000675141.1:c.1852G= ENSP00000502420.1:p.Ala618=
ENST00000675198.1:n.1831G=
ENST00000675213.1:c.1906G= ENSP00000502218.1:p.Ala636=
ENST00000675224.1:c.*17G= ENSP00000501869.1:n.*17G=
ENST00000675253.1:c.*623G= ENSP00000502557.1:n.*623G=
ENST00000675445.1:c.*1623G= ENSP00000502253.1:n.*1623G=
ENST00000675448.1:c.1951G= ENSP00000502167.1:p.Ala651=
ENST00000675521.1:n.1861G=
ENST00000675572.1:c.1852G= ENSP00000501598.1:p.Ala618=
ENST00000675641.1:c.*693G= ENSP00000501845.1:n.*693G=
ENST00000675657.1:c.*564G= ENSP00000502002.1:n.*564G=
ENST00000675662.1:n.1746G=
ENST00000675789.1:c.1771G= ENSP00000501954.1:p.Ala591=
ENST00000675883.1:c.1870G= ENSP00000501592.1:p.Ala624=
ENST00000675945.1:c.*592G= ENSP00000501835.1:n.*592G=
ENST00000676014.1:c.1894G= ENSP00000502058.1:p.Ala632=
ENST00000676035.1:n.1613G=
ENST00000676106.1:n.1988G=
ENST00000676137.1:n.1981G=
ENST00000676170.1:c.2032G= ENSP00000502177.1:p.Ala678=
ENST00000676318.1:c.*2781G= ENSP00000502300.1:n.*2781G=
ENST00000676336.1:c.*564G= ENSP00000502686.1:n.*564G=
ENST00000676349.1:c.*1639G= ENSP00000502155.1:n.*1639G=
ENST00000676399.1:n.1854G=
ENST00000676409.1:n.2011G=
ENST00000300417.10:c.1951G= ENSP00000300417.6:p.Ala651=
ENST00000323301.8:c.1951G= ENSP00000322937.4:p.Ala651=
ENST00000373322.1:c.1951G= ENSP00000362419.1:p.Ala651=
ENST00000373324.8:c.1870G= ENSP00000362421.4:p.Ala624=
ENST00000472068.1:n.844G=
ENST00000483302.5:n.1173G=
NM_001005373.3:c.1951G= NP_001005373.1:p.Ala651=
NM_001005374.3:c.1951G= NP_001005374.1:p.Ala651=
NM_001190723.2:c.1870G= NP_001177652.1:p.Ala624=
NM_138361.5:c.1951G= , LRG_373t1:c.1951G= NP_612370.3:p.Ala651=
XM_006717316.2:c.1852G= XP_006717379.1:p.Ala618=
XM_006717316.4:c.1852G= XP_006717379.1:p.Ala618=
XM_017015283.1:c.1951G= XP_016870772.1:p.Ala651=
XM_017015284.2:c.1162G= XP_016870773.1:p.Ala388=
XR_001746415.2:n.2486G=
XR_929874.3:n.2310G=
NM_001190723.3:c.1870G= NP_001177652.1:p.Ala624=
NM_001005373.4:c.1951G= MANE Select NP_001005373.1:p.Ala651=
NM_001005374.4:c.1951G= NP_001005374.1:p.Ala651=
NM_001384142.1:c.1951G= NP_001371071.1:p.Ala651=
NM_001384143.1:c.1852G= NP_001371072.1:p.Ala618=
NM_001384144.1:c.1162G= NP_001371073.1:p.Ala388=
NR_168891.1:n.2480G=
NR_168892.1:n.2304G=