Canonical Allele Identifier: CA1879828644
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501071T= , CM000671.2:g.127501071T= GRCh38
NC_000009.11:g.130263350T= , CM000671.1:g.130263350T= GRCh37
NC_000009.10:g.129303171T= NCBI36
NG_032008.1:g.54586T= , LRG_373:g.54586T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1974T= MANE Select ENSP00000300417.6:p.Ser658=
ENST00000472068.2:c.*1698T= ENSP00000501555.1:n.*1698T=
ENST00000483302.6:n.2639T=
ENST00000498513.6:c.*865T= ENSP00000501637.1:n.*865T=
ENST00000674511.1:n.1573T=
ENST00000674516.1:c.*590T= ENSP00000502441.1:n.*590T=
ENST00000674621.1:n.1861-2302T=
ENST00000674771.1:c.*617T= ENSP00000502627.1:n.*617T=
ENST00000674784.1:c.*1034T= ENSP00000501837.1:n.*1034T=
ENST00000674970.1:c.*1748T= ENSP00000502493.1:n.*1748T=
ENST00000675012.1:n.1918T=
ENST00000675141.1:c.1875T= ENSP00000502420.1:p.Ser625=
ENST00000675198.1:n.1854T=
ENST00000675213.1:c.1929T= ENSP00000502218.1:p.Ser643=
ENST00000675224.1:c.*40T= ENSP00000501869.1:n.*40T=
ENST00000675253.1:c.*646T= ENSP00000502557.1:n.*646T=
ENST00000675445.1:c.*1646T= ENSP00000502253.1:n.*1646T=
ENST00000675448.1:c.1974T= ENSP00000502167.1:p.Ser658=
ENST00000675521.1:n.1884T=
ENST00000675572.1:c.1875T= ENSP00000501598.1:p.Ser625=
ENST00000675641.1:c.*716T= ENSP00000501845.1:n.*716T=
ENST00000675657.1:c.*587T= ENSP00000502002.1:n.*587T=
ENST00000675662.1:n.1769T=
ENST00000675789.1:c.1794T= ENSP00000501954.1:p.Ser598=
ENST00000675883.1:c.1893T= ENSP00000501592.1:p.Ser631=
ENST00000675945.1:c.*615T= ENSP00000501835.1:n.*615T=
ENST00000676014.1:c.1917T= ENSP00000502058.1:p.Ser639=
ENST00000676035.1:n.1636T=
ENST00000676106.1:n.2011T=
ENST00000676137.1:n.2004T=
ENST00000676170.1:c.2055T= ENSP00000502177.1:p.Ser685=
ENST00000676318.1:c.*2804T= ENSP00000502300.1:n.*2804T=
ENST00000676336.1:c.*587T= ENSP00000502686.1:n.*587T=
ENST00000676349.1:c.*1662T= ENSP00000502155.1:n.*1662T=
ENST00000676399.1:n.1877T=
ENST00000676409.1:n.2034T=
ENST00000300417.10:c.1974T= ENSP00000300417.6:p.Ser658=
ENST00000323301.8:c.1974T= ENSP00000322937.4:p.Ser658=
ENST00000373322.1:c.1974T= ENSP00000362419.1:p.Ser658=
ENST00000373324.8:c.1893T= ENSP00000362421.4:p.Ser631=
ENST00000483302.5:n.1196T=
NM_001005373.3:c.1974T= NP_001005373.1:p.Ser658=
NM_001005374.3:c.1974T= NP_001005374.1:p.Ser658=
NM_001190723.2:c.1893T= NP_001177652.1:p.Ser631=
NM_138361.5:c.1974T= , LRG_373t1:c.1974T= NP_612370.3:p.Ser658=
XM_006717316.2:c.1875T= XP_006717379.1:p.Ser625=
XM_006717316.4:c.1875T= XP_006717379.1:p.Ser625=
XM_017015283.1:c.1974T= XP_016870772.1:p.Ser658=
XM_017015284.2:c.1185T= XP_016870773.1:p.Ser395=
XR_001746415.2:n.2509T=
XR_929874.3:n.2333T=
NM_001190723.3:c.1893T= NP_001177652.1:p.Ser631=
NM_001005373.4:c.1974T= MANE Select NP_001005373.1:p.Ser658=
NM_001005374.4:c.1974T= NP_001005374.1:p.Ser658=
NM_001384142.1:c.1974T= NP_001371071.1:p.Ser658=
NM_001384143.1:c.1875T= NP_001371072.1:p.Ser625=
NM_001384144.1:c.1185T= NP_001371073.1:p.Ser395=
NR_168891.1:n.2503T=
NR_168892.1:n.2327T=