Canonical Allele Identifier: CA1879828511
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501033G= , CM000671.2:g.127501033G= GRCh38
NC_000009.11:g.130263312G= , CM000671.1:g.130263312G= GRCh37
NC_000009.10:g.129303133G= NCBI36
NG_032008.1:g.54548G= , LRG_373:g.54548G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1936G= MANE Select ENSP00000300417.6:p.Val646=
ENST00000472068.2:c.*1660G= ENSP00000501555.1:n.*1660G=
ENST00000483302.6:n.2601G=
ENST00000498513.6:c.*827G= ENSP00000501637.1:n.*827G=
ENST00000674511.1:n.1535G=
ENST00000674516.1:c.*552G= ENSP00000502441.1:n.*552G=
ENST00000674621.1:n.1861-2340G=
ENST00000674771.1:c.*579G= ENSP00000502627.1:n.*579G=
ENST00000674784.1:c.*996G= ENSP00000501837.1:n.*996G=
ENST00000674970.1:c.*1710G= ENSP00000502493.1:n.*1710G=
ENST00000675012.1:n.1880G=
ENST00000675141.1:c.1837G= ENSP00000502420.1:p.Val613=
ENST00000675198.1:n.1816G=
ENST00000675213.1:c.1891G= ENSP00000502218.1:p.Val631=
ENST00000675224.1:c.*2G= ENSP00000501869.1:n.*2G=
ENST00000675253.1:c.*608G= ENSP00000502557.1:n.*608G=
ENST00000675445.1:c.*1608G= ENSP00000502253.1:n.*1608G=
ENST00000675448.1:c.1936G= ENSP00000502167.1:p.Val646=
ENST00000675521.1:n.1846G=
ENST00000675572.1:c.1837G= ENSP00000501598.1:p.Val613=
ENST00000675641.1:c.*678G= ENSP00000501845.1:n.*678G=
ENST00000675657.1:c.*549G= ENSP00000502002.1:n.*549G=
ENST00000675662.1:n.1731G=
ENST00000675789.1:c.1756G= ENSP00000501954.1:p.Val586=
ENST00000675883.1:c.1855G= ENSP00000501592.1:p.Val619=
ENST00000675945.1:c.*577G= ENSP00000501835.1:n.*577G=
ENST00000676014.1:c.1879G= ENSP00000502058.1:p.Val627=
ENST00000676035.1:n.1598G=
ENST00000676106.1:n.1973G=
ENST00000676137.1:n.1966G=
ENST00000676170.1:c.2017G= ENSP00000502177.1:p.Val673=
ENST00000676318.1:c.*2766G= ENSP00000502300.1:n.*2766G=
ENST00000676336.1:c.*549G= ENSP00000502686.1:n.*549G=
ENST00000676349.1:c.*1624G= ENSP00000502155.1:n.*1624G=
ENST00000676399.1:n.1839G=
ENST00000676409.1:n.1996G=
ENST00000300417.10:c.1936G= ENSP00000300417.6:p.Val646=
ENST00000323301.8:c.1936G= ENSP00000322937.4:p.Val646=
ENST00000373322.1:c.1936G= ENSP00000362419.1:p.Val646=
ENST00000373324.8:c.1855G= ENSP00000362421.4:p.Val619=
ENST00000472068.1:n.829G=
ENST00000483302.5:n.1158G=
NM_001005373.3:c.1936G= NP_001005373.1:p.Val646=
NM_001005374.3:c.1936G= NP_001005374.1:p.Val646=
NM_001190723.2:c.1855G= NP_001177652.1:p.Val619=
NM_138361.5:c.1936G= , LRG_373t1:c.1936G= NP_612370.3:p.Val646=
XM_006717316.2:c.1837G= XP_006717379.1:p.Val613=
XM_006717316.4:c.1837G= XP_006717379.1:p.Val613=
XM_017015283.1:c.1936G= XP_016870772.1:p.Val646=
XM_017015284.2:c.1147G= XP_016870773.1:p.Val383=
XR_001746415.2:n.2471G=
XR_929874.3:n.2295G=
NM_001190723.3:c.1855G= NP_001177652.1:p.Val619=
NM_001005373.4:c.1936G= MANE Select NP_001005373.1:p.Val646=
NM_001005374.4:c.1936G= NP_001005374.1:p.Val646=
NM_001384142.1:c.1936G= NP_001371071.1:p.Val646=
NM_001384143.1:c.1837G= NP_001371072.1:p.Val613=
NM_001384144.1:c.1147G= NP_001371073.1:p.Val383=
NR_168891.1:n.2465G=
NR_168892.1:n.2289G=