Canonical Allele Identifier: CA1879828556
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501046C= , CM000671.2:g.127501046C= GRCh38
NC_000009.11:g.130263325C= , CM000671.1:g.130263325C= GRCh37
NC_000009.10:g.129303146C= NCBI36
NG_032008.1:g.54561C= , LRG_373:g.54561C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1949C= MANE Select ENSP00000300417.6:p.Thr650=
ENST00000472068.2:c.*1673C= ENSP00000501555.1:n.*1673C=
ENST00000483302.6:n.2614C=
ENST00000498513.6:c.*840C= ENSP00000501637.1:n.*840C=
ENST00000674511.1:n.1548C=
ENST00000674516.1:c.*565C= ENSP00000502441.1:n.*565C=
ENST00000674621.1:n.1861-2327C=
ENST00000674771.1:c.*592C= ENSP00000502627.1:n.*592C=
ENST00000674784.1:c.*1009C= ENSP00000501837.1:n.*1009C=
ENST00000674970.1:c.*1723C= ENSP00000502493.1:n.*1723C=
ENST00000675012.1:n.1893C=
ENST00000675141.1:c.1850C= ENSP00000502420.1:p.Thr617=
ENST00000675198.1:n.1829C=
ENST00000675213.1:c.1904C= ENSP00000502218.1:p.Thr635=
ENST00000675224.1:c.*15C= ENSP00000501869.1:n.*15C=
ENST00000675253.1:c.*621C= ENSP00000502557.1:n.*621C=
ENST00000675445.1:c.*1621C= ENSP00000502253.1:n.*1621C=
ENST00000675448.1:c.1949C= ENSP00000502167.1:p.Thr650=
ENST00000675521.1:n.1859C=
ENST00000675572.1:c.1850C= ENSP00000501598.1:p.Thr617=
ENST00000675641.1:c.*691C= ENSP00000501845.1:n.*691C=
ENST00000675657.1:c.*562C= ENSP00000502002.1:n.*562C=
ENST00000675662.1:n.1744C=
ENST00000675789.1:c.1769C= ENSP00000501954.1:p.Thr590=
ENST00000675883.1:c.1868C= ENSP00000501592.1:p.Thr623=
ENST00000675945.1:c.*590C= ENSP00000501835.1:n.*590C=
ENST00000676014.1:c.1892C= ENSP00000502058.1:p.Thr631=
ENST00000676035.1:n.1611C=
ENST00000676106.1:n.1986C=
ENST00000676137.1:n.1979C=
ENST00000676170.1:c.2030C= ENSP00000502177.1:p.Thr677=
ENST00000676318.1:c.*2779C= ENSP00000502300.1:n.*2779C=
ENST00000676336.1:c.*562C= ENSP00000502686.1:n.*562C=
ENST00000676349.1:c.*1637C= ENSP00000502155.1:n.*1637C=
ENST00000676399.1:n.1852C=
ENST00000676409.1:n.2009C=
ENST00000300417.10:c.1949C= ENSP00000300417.6:p.Thr650=
ENST00000323301.8:c.1949C= ENSP00000322937.4:p.Thr650=
ENST00000373322.1:c.1949C= ENSP00000362419.1:p.Thr650=
ENST00000373324.8:c.1868C= ENSP00000362421.4:p.Thr623=
ENST00000472068.1:n.842C=
ENST00000483302.5:n.1171C=
NM_001005373.3:c.1949C= NP_001005373.1:p.Thr650=
NM_001005374.3:c.1949C= NP_001005374.1:p.Thr650=
NM_001190723.2:c.1868C= NP_001177652.1:p.Thr623=
NM_138361.5:c.1949C= , LRG_373t1:c.1949C= NP_612370.3:p.Thr650=
XM_006717316.2:c.1850C= XP_006717379.1:p.Thr617=
XM_006717316.4:c.1850C= XP_006717379.1:p.Thr617=
XM_017015283.1:c.1949C= XP_016870772.1:p.Thr650=
XM_017015284.2:c.1160C= XP_016870773.1:p.Thr387=
XR_001746415.2:n.2484C=
XR_929874.3:n.2308C=
NM_001190723.3:c.1868C= NP_001177652.1:p.Thr623=
NM_001005373.4:c.1949C= MANE Select NP_001005373.1:p.Thr650=
NM_001005374.4:c.1949C= NP_001005374.1:p.Thr650=
NM_001384142.1:c.1949C= NP_001371071.1:p.Thr650=
NM_001384143.1:c.1850C= NP_001371072.1:p.Thr617=
NM_001384144.1:c.1160C= NP_001371073.1:p.Thr387=
NR_168891.1:n.2478C=
NR_168892.1:n.2302C=