Canonical Allele Identifier: CA1879828691
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501083C= , CM000671.2:g.127501083C= GRCh38
NC_000009.11:g.130263362C= , CM000671.1:g.130263362C= GRCh37
NC_000009.10:g.129303183C= NCBI36
NG_032008.1:g.54598C= , LRG_373:g.54598C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1986C= MANE Select ENSP00000300417.6:p.Ser662=
ENST00000472068.2:c.*1710C= ENSP00000501555.1:n.*1710C=
ENST00000483302.6:n.2651C=
ENST00000498513.6:c.*877C= ENSP00000501637.1:n.*877C=
ENST00000674511.1:n.1585C=
ENST00000674516.1:c.*602C= ENSP00000502441.1:n.*602C=
ENST00000674621.1:n.1861-2290C=
ENST00000674771.1:c.*629C= ENSP00000502627.1:n.*629C=
ENST00000674784.1:c.*1046C= ENSP00000501837.1:n.*1046C=
ENST00000674970.1:c.*1760C= ENSP00000502493.1:n.*1760C=
ENST00000675012.1:n.1930C=
ENST00000675141.1:c.1887C= ENSP00000502420.1:p.Ser629=
ENST00000675198.1:n.1866C=
ENST00000675213.1:c.1941C= ENSP00000502218.1:p.Ser647=
ENST00000675224.1:c.*52C= ENSP00000501869.1:n.*52C=
ENST00000675253.1:c.*658C= ENSP00000502557.1:n.*658C=
ENST00000675445.1:c.*1658C= ENSP00000502253.1:n.*1658C=
ENST00000675448.1:c.1986C= ENSP00000502167.1:p.Ser662=
ENST00000675521.1:n.1896C=
ENST00000675572.1:c.1887C= ENSP00000501598.1:p.Ser629=
ENST00000675641.1:c.*728C= ENSP00000501845.1:n.*728C=
ENST00000675657.1:c.*599C= ENSP00000502002.1:n.*599C=
ENST00000675662.1:n.1781C=
ENST00000675789.1:c.1806C= ENSP00000501954.1:p.Ser602=
ENST00000675883.1:c.1905C= ENSP00000501592.1:p.Ser635=
ENST00000675945.1:c.*627C= ENSP00000501835.1:n.*627C=
ENST00000676014.1:c.1929C= ENSP00000502058.1:p.Ser643=
ENST00000676035.1:n.1648C=
ENST00000676106.1:n.2023C=
ENST00000676137.1:n.2016C=
ENST00000676170.1:c.2067C= ENSP00000502177.1:p.Ser689=
ENST00000676318.1:c.*2816C= ENSP00000502300.1:n.*2816C=
ENST00000676336.1:c.*599C= ENSP00000502686.1:n.*599C=
ENST00000676349.1:c.*1674C= ENSP00000502155.1:n.*1674C=
ENST00000676399.1:n.1889C=
ENST00000676409.1:n.2046C=
ENST00000300417.10:c.1986C= ENSP00000300417.6:p.Ser662=
ENST00000323301.8:c.1986C= ENSP00000322937.4:p.Ser662=
ENST00000373322.1:c.1986C= ENSP00000362419.1:p.Ser662=
ENST00000373324.8:c.1905C= ENSP00000362421.4:p.Ser635=
ENST00000483302.5:n.1208C=
NM_001005373.3:c.1986C= NP_001005373.1:p.Ser662=
NM_001005374.3:c.1986C= NP_001005374.1:p.Ser662=
NM_001190723.2:c.1905C= NP_001177652.1:p.Ser635=
NM_138361.5:c.1986C= , LRG_373t1:c.1986C= NP_612370.3:p.Ser662=
XM_006717316.2:c.1887C= XP_006717379.1:p.Ser629=
XM_006717316.4:c.1887C= XP_006717379.1:p.Ser629=
XM_017015283.1:c.1986C= XP_016870772.1:p.Ser662=
XM_017015284.2:c.1197C= XP_016870773.1:p.Ser399=
XR_001746415.2:n.2521C=
XR_929874.3:n.2345C=
NM_001190723.3:c.1905C= NP_001177652.1:p.Ser635=
NM_001005373.4:c.1986C= MANE Select NP_001005373.1:p.Ser662=
NM_001005374.4:c.1986C= NP_001005374.1:p.Ser662=
NM_001384142.1:c.1986C= NP_001371071.1:p.Ser662=
NM_001384143.1:c.1887C= NP_001371072.1:p.Ser629=
NM_001384144.1:c.1197C= NP_001371073.1:p.Ser399=
NR_168891.1:n.2515C=
NR_168892.1:n.2339C=