Canonical Allele Identifier: CA1879828699
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501085C= , CM000671.2:g.127501085C= GRCh38
NC_000009.11:g.130263364C= , CM000671.1:g.130263364C= GRCh37
NC_000009.10:g.129303185C= NCBI36
NG_032008.1:g.54600C= , LRG_373:g.54600C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1988C= MANE Select ENSP00000300417.6:p.Ala663=
ENST00000472068.2:c.*1712C= ENSP00000501555.1:n.*1712C=
ENST00000483302.6:n.2653C=
ENST00000498513.6:c.*879C= ENSP00000501637.1:n.*879C=
ENST00000674511.1:n.1587C=
ENST00000674516.1:c.*604C= ENSP00000502441.1:n.*604C=
ENST00000674621.1:n.1861-2288C=
ENST00000674771.1:c.*631C= ENSP00000502627.1:n.*631C=
ENST00000674784.1:c.*1048C= ENSP00000501837.1:n.*1048C=
ENST00000674970.1:c.*1762C= ENSP00000502493.1:n.*1762C=
ENST00000675012.1:n.1932C=
ENST00000675141.1:c.1889C= ENSP00000502420.1:p.Ala630=
ENST00000675198.1:n.1868C=
ENST00000675213.1:c.1943C= ENSP00000502218.1:p.Ala648=
ENST00000675224.1:c.*54C= ENSP00000501869.1:n.*54C=
ENST00000675253.1:c.*660C= ENSP00000502557.1:n.*660C=
ENST00000675445.1:c.*1660C= ENSP00000502253.1:n.*1660C=
ENST00000675448.1:c.1988C= ENSP00000502167.1:p.Ala663=
ENST00000675521.1:n.1898C=
ENST00000675572.1:c.1889C= ENSP00000501598.1:p.Ala630=
ENST00000675641.1:c.*730C= ENSP00000501845.1:n.*730C=
ENST00000675657.1:c.*601C= ENSP00000502002.1:n.*601C=
ENST00000675662.1:n.1783C=
ENST00000675789.1:c.1808C= ENSP00000501954.1:p.Ala603=
ENST00000675883.1:c.1907C= ENSP00000501592.1:p.Ala636=
ENST00000675945.1:c.*629C= ENSP00000501835.1:n.*629C=
ENST00000676014.1:c.1931C= ENSP00000502058.1:p.Ala644=
ENST00000676035.1:n.1650C=
ENST00000676106.1:n.2025C=
ENST00000676137.1:n.2018C=
ENST00000676170.1:c.2069C= ENSP00000502177.1:p.Ala690=
ENST00000676318.1:c.*2818C= ENSP00000502300.1:n.*2818C=
ENST00000676336.1:c.*601C= ENSP00000502686.1:n.*601C=
ENST00000676349.1:c.*1676C= ENSP00000502155.1:n.*1676C=
ENST00000676399.1:n.1891C=
ENST00000676409.1:n.2048C=
ENST00000300417.10:c.1988C= ENSP00000300417.6:p.Ala663=
ENST00000323301.8:c.1988C= ENSP00000322937.4:p.Ala663=
ENST00000373322.1:c.1988C= ENSP00000362419.1:p.Ala663=
ENST00000373324.8:c.1907C= ENSP00000362421.4:p.Ala636=
ENST00000483302.5:n.1210C=
NM_001005373.3:c.1988C= NP_001005373.1:p.Ala663=
NM_001005374.3:c.1988C= NP_001005374.1:p.Ala663=
NM_001190723.2:c.1907C= NP_001177652.1:p.Ala636=
NM_138361.5:c.1988C= , LRG_373t1:c.1988C= NP_612370.3:p.Ala663=
XM_006717316.2:c.1889C= XP_006717379.1:p.Ala630=
XM_006717316.4:c.1889C= XP_006717379.1:p.Ala630=
XM_017015283.1:c.1988C= XP_016870772.1:p.Ala663=
XM_017015284.2:c.1199C= XP_016870773.1:p.Ala400=
XR_001746415.2:n.2523C=
XR_929874.3:n.2347C=
NM_001190723.3:c.1907C= NP_001177652.1:p.Ala636=
NM_001005373.4:c.1988C= MANE Select NP_001005373.1:p.Ala663=
NM_001005374.4:c.1988C= NP_001005374.1:p.Ala663=
NM_001384142.1:c.1988C= NP_001371071.1:p.Ala663=
NM_001384143.1:c.1889C= NP_001371072.1:p.Ala630=
NM_001384144.1:c.1199C= NP_001371073.1:p.Ala400=
NR_168891.1:n.2517C=
NR_168892.1:n.2341C=