Canonical Allele Identifier: CA1879828529
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501037T= , CM000671.2:g.127501037T= GRCh38
NC_000009.11:g.130263316T= , CM000671.1:g.130263316T= GRCh37
NC_000009.10:g.129303137T= NCBI36
NG_032008.1:g.54552T= , LRG_373:g.54552T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1940T= MANE Select ENSP00000300417.6:p.Val647=
ENST00000472068.2:c.*1664T= ENSP00000501555.1:n.*1664T=
ENST00000483302.6:n.2605T=
ENST00000498513.6:c.*831T= ENSP00000501637.1:n.*831T=
ENST00000674511.1:n.1539T=
ENST00000674516.1:c.*556T= ENSP00000502441.1:n.*556T=
ENST00000674621.1:n.1861-2336T=
ENST00000674771.1:c.*583T= ENSP00000502627.1:n.*583T=
ENST00000674784.1:c.*1000T= ENSP00000501837.1:n.*1000T=
ENST00000674970.1:c.*1714T= ENSP00000502493.1:n.*1714T=
ENST00000675012.1:n.1884T=
ENST00000675141.1:c.1841T= ENSP00000502420.1:p.Val614=
ENST00000675198.1:n.1820T=
ENST00000675213.1:c.1895T= ENSP00000502218.1:p.Val632=
ENST00000675224.1:c.*6T= ENSP00000501869.1:n.*6T=
ENST00000675253.1:c.*612T= ENSP00000502557.1:n.*612T=
ENST00000675445.1:c.*1612T= ENSP00000502253.1:n.*1612T=
ENST00000675448.1:c.1940T= ENSP00000502167.1:p.Val647=
ENST00000675521.1:n.1850T=
ENST00000675572.1:c.1841T= ENSP00000501598.1:p.Val614=
ENST00000675641.1:c.*682T= ENSP00000501845.1:n.*682T=
ENST00000675657.1:c.*553T= ENSP00000502002.1:n.*553T=
ENST00000675662.1:n.1735T=
ENST00000675789.1:c.1760T= ENSP00000501954.1:p.Val587=
ENST00000675883.1:c.1859T= ENSP00000501592.1:p.Val620=
ENST00000675945.1:c.*581T= ENSP00000501835.1:n.*581T=
ENST00000676014.1:c.1883T= ENSP00000502058.1:p.Val628=
ENST00000676035.1:n.1602T=
ENST00000676106.1:n.1977T=
ENST00000676137.1:n.1970T=
ENST00000676170.1:c.2021T= ENSP00000502177.1:p.Val674=
ENST00000676318.1:c.*2770T= ENSP00000502300.1:n.*2770T=
ENST00000676336.1:c.*553T= ENSP00000502686.1:n.*553T=
ENST00000676349.1:c.*1628T= ENSP00000502155.1:n.*1628T=
ENST00000676399.1:n.1843T=
ENST00000676409.1:n.2000T=
ENST00000300417.10:c.1940T= ENSP00000300417.6:p.Val647=
ENST00000323301.8:c.1940T= ENSP00000322937.4:p.Val647=
ENST00000373322.1:c.1940T= ENSP00000362419.1:p.Val647=
ENST00000373324.8:c.1859T= ENSP00000362421.4:p.Val620=
ENST00000472068.1:n.833T=
ENST00000483302.5:n.1162T=
NM_001005373.3:c.1940T= NP_001005373.1:p.Val647=
NM_001005374.3:c.1940T= NP_001005374.1:p.Val647=
NM_001190723.2:c.1859T= NP_001177652.1:p.Val620=
NM_138361.5:c.1940T= , LRG_373t1:c.1940T= NP_612370.3:p.Val647=
XM_006717316.2:c.1841T= XP_006717379.1:p.Val614=
XM_006717316.4:c.1841T= XP_006717379.1:p.Val614=
XM_017015283.1:c.1940T= XP_016870772.1:p.Val647=
XM_017015284.2:c.1151T= XP_016870773.1:p.Val384=
XR_001746415.2:n.2475T=
XR_929874.3:n.2299T=
NM_001190723.3:c.1859T= NP_001177652.1:p.Val620=
NM_001005373.4:c.1940T= MANE Select NP_001005373.1:p.Val647=
NM_001005374.4:c.1940T= NP_001005374.1:p.Val647=
NM_001384142.1:c.1940T= NP_001371071.1:p.Val647=
NM_001384143.1:c.1841T= NP_001371072.1:p.Val614=
NM_001384144.1:c.1151T= NP_001371073.1:p.Val384=
NR_168891.1:n.2469T=
NR_168892.1:n.2293T=