Canonical Allele Identifier: CA1879828694
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501084G= , CM000671.2:g.127501084G= GRCh38
NC_000009.11:g.130263363G= , CM000671.1:g.130263363G= GRCh37
NC_000009.10:g.129303184G= NCBI36
NG_032008.1:g.54599G= , LRG_373:g.54599G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1987G= MANE Select ENSP00000300417.6:p.Ala663=
ENST00000472068.2:c.*1711G= ENSP00000501555.1:n.*1711G=
ENST00000483302.6:n.2652G=
ENST00000498513.6:c.*878G= ENSP00000501637.1:n.*878G=
ENST00000674511.1:n.1586G=
ENST00000674516.1:c.*603G= ENSP00000502441.1:n.*603G=
ENST00000674621.1:n.1861-2289G=
ENST00000674771.1:c.*630G= ENSP00000502627.1:n.*630G=
ENST00000674784.1:c.*1047G= ENSP00000501837.1:n.*1047G=
ENST00000674970.1:c.*1761G= ENSP00000502493.1:n.*1761G=
ENST00000675012.1:n.1931G=
ENST00000675141.1:c.1888G= ENSP00000502420.1:p.Ala630=
ENST00000675198.1:n.1867G=
ENST00000675213.1:c.1942G= ENSP00000502218.1:p.Ala648=
ENST00000675224.1:c.*53G= ENSP00000501869.1:n.*53G=
ENST00000675253.1:c.*659G= ENSP00000502557.1:n.*659G=
ENST00000675445.1:c.*1659G= ENSP00000502253.1:n.*1659G=
ENST00000675448.1:c.1987G= ENSP00000502167.1:p.Ala663=
ENST00000675521.1:n.1897G=
ENST00000675572.1:c.1888G= ENSP00000501598.1:p.Ala630=
ENST00000675641.1:c.*729G= ENSP00000501845.1:n.*729G=
ENST00000675657.1:c.*600G= ENSP00000502002.1:n.*600G=
ENST00000675662.1:n.1782G=
ENST00000675789.1:c.1807G= ENSP00000501954.1:p.Ala603=
ENST00000675883.1:c.1906G= ENSP00000501592.1:p.Ala636=
ENST00000675945.1:c.*628G= ENSP00000501835.1:n.*628G=
ENST00000676014.1:c.1930G= ENSP00000502058.1:p.Ala644=
ENST00000676035.1:n.1649G=
ENST00000676106.1:n.2024G=
ENST00000676137.1:n.2017G=
ENST00000676170.1:c.2068G= ENSP00000502177.1:p.Ala690=
ENST00000676318.1:c.*2817G= ENSP00000502300.1:n.*2817G=
ENST00000676336.1:c.*600G= ENSP00000502686.1:n.*600G=
ENST00000676349.1:c.*1675G= ENSP00000502155.1:n.*1675G=
ENST00000676399.1:n.1890G=
ENST00000676409.1:n.2047G=
ENST00000300417.10:c.1987G= ENSP00000300417.6:p.Ala663=
ENST00000323301.8:c.1987G= ENSP00000322937.4:p.Ala663=
ENST00000373322.1:c.1987G= ENSP00000362419.1:p.Ala663=
ENST00000373324.8:c.1906G= ENSP00000362421.4:p.Ala636=
ENST00000483302.5:n.1209G=
NM_001005373.3:c.1987G= NP_001005373.1:p.Ala663=
NM_001005374.3:c.1987G= NP_001005374.1:p.Ala663=
NM_001190723.2:c.1906G= NP_001177652.1:p.Ala636=
NM_138361.5:c.1987G= , LRG_373t1:c.1987G= NP_612370.3:p.Ala663=
XM_006717316.2:c.1888G= XP_006717379.1:p.Ala630=
XM_006717316.4:c.1888G= XP_006717379.1:p.Ala630=
XM_017015283.1:c.1987G= XP_016870772.1:p.Ala663=
XM_017015284.2:c.1198G= XP_016870773.1:p.Ala400=
XR_001746415.2:n.2522G=
XR_929874.3:n.2346G=
NM_001190723.3:c.1906G= NP_001177652.1:p.Ala636=
NM_001005373.4:c.1987G= MANE Select NP_001005373.1:p.Ala663=
NM_001005374.4:c.1987G= NP_001005374.1:p.Ala663=
NM_001384142.1:c.1987G= NP_001371071.1:p.Ala663=
NM_001384143.1:c.1888G= NP_001371072.1:p.Ala630=
NM_001384144.1:c.1198G= NP_001371073.1:p.Ala400=
NR_168891.1:n.2516G=
NR_168892.1:n.2340G=