Canonical Allele Identifier: CA1879828792
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501115C= , CM000671.2:g.127501115C= GRCh38
NC_000009.11:g.130263394C= , CM000671.1:g.130263394C= GRCh37
NC_000009.10:g.129303215C= NCBI36
NG_032008.1:g.54630C= , LRG_373:g.54630C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.2018C= MANE Select ENSP00000300417.6:p.Ser673=
ENST00000472068.2:c.*1742C= ENSP00000501555.1:n.*1742C=
ENST00000483302.6:n.2683C=
ENST00000498513.6:c.*909C= ENSP00000501637.1:n.*909C=
ENST00000674511.1:n.1617C=
ENST00000674516.1:c.*634C= ENSP00000502441.1:n.*634C=
ENST00000674621.1:n.1861-2258C=
ENST00000674771.1:c.*661C= ENSP00000502627.1:n.*661C=
ENST00000674784.1:c.*1078C= ENSP00000501837.1:n.*1078C=
ENST00000674970.1:c.*1792C= ENSP00000502493.1:n.*1792C=
ENST00000675012.1:n.1962C=
ENST00000675141.1:c.1919C= ENSP00000502420.1:p.Ser640=
ENST00000675198.1:n.1898C=
ENST00000675213.1:c.1973C= ENSP00000502218.1:p.Ser658=
ENST00000675224.1:c.*84C= ENSP00000501869.1:n.*84C=
ENST00000675253.1:c.*690C= ENSP00000502557.1:n.*690C=
ENST00000675445.1:c.*1690C= ENSP00000502253.1:n.*1690C=
ENST00000675448.1:c.2018C= ENSP00000502167.1:p.Ser673=
ENST00000675521.1:n.1928C=
ENST00000675572.1:c.1919C= ENSP00000501598.1:p.Ser640=
ENST00000675641.1:c.*760C= ENSP00000501845.1:n.*760C=
ENST00000675657.1:c.*631C= ENSP00000502002.1:n.*631C=
ENST00000675662.1:n.1813C=
ENST00000675789.1:c.1838C= ENSP00000501954.1:p.Ser613=
ENST00000675883.1:c.1937C= ENSP00000501592.1:p.Ser646=
ENST00000675945.1:c.*659C= ENSP00000501835.1:n.*659C=
ENST00000676014.1:c.1961C= ENSP00000502058.1:p.Ser654=
ENST00000676035.1:n.1680C=
ENST00000676106.1:n.2055C=
ENST00000676137.1:n.2048C=
ENST00000676170.1:c.2099C= ENSP00000502177.1:p.Ser700=
ENST00000676318.1:c.*2848C= ENSP00000502300.1:n.*2848C=
ENST00000676336.1:c.*631C= ENSP00000502686.1:n.*631C=
ENST00000676349.1:c.*1706C= ENSP00000502155.1:n.*1706C=
ENST00000676399.1:n.1921C=
ENST00000676409.1:n.2078C=
ENST00000300417.10:c.2018C= ENSP00000300417.6:p.Ser673=
ENST00000323301.8:c.2018C= ENSP00000322937.4:p.Ser673=
ENST00000373322.1:c.2018C= ENSP00000362419.1:p.Ser673=
ENST00000373324.8:c.1937C= ENSP00000362421.4:p.Ser646=
ENST00000483302.5:n.1240C=
NM_001005373.3:c.2018C= NP_001005373.1:p.Ser673=
NM_001005374.3:c.2018C= NP_001005374.1:p.Ser673=
NM_001190723.2:c.1937C= NP_001177652.1:p.Ser646=
NM_138361.5:c.2018C= , LRG_373t1:c.2018C= NP_612370.3:p.Ser673=
XM_006717316.2:c.1919C= XP_006717379.1:p.Ser640=
XM_006717316.4:c.1919C= XP_006717379.1:p.Ser640=
XM_017015283.1:c.2018C= XP_016870772.1:p.Ser673=
XM_017015284.2:c.1229C= XP_016870773.1:p.Ser410=
XR_001746415.2:n.2553C=
XR_929874.3:n.2377C=
NM_001190723.3:c.1937C= NP_001177652.1:p.Ser646=
NM_001005373.4:c.2018C= MANE Select NP_001005373.1:p.Ser673=
NM_001005374.4:c.2018C= NP_001005374.1:p.Ser673=
NM_001384142.1:c.2018C= NP_001371071.1:p.Ser673=
NM_001384143.1:c.1919C= NP_001371072.1:p.Ser640=
NM_001384144.1:c.1229C= NP_001371073.1:p.Ser410=
NR_168891.1:n.2547C=
NR_168892.1:n.2371C=