Canonical Allele Identifier: CA1879828801
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501116A= , CM000671.2:g.127501116A= GRCh38
NC_000009.11:g.130263395A= , CM000671.1:g.130263395A= GRCh37
NC_000009.10:g.129303216A= NCBI36
NG_032008.1:g.54631A= , LRG_373:g.54631A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.2019A= MANE Select ENSP00000300417.6:p.Ser673=
ENST00000472068.2:c.*1743A= ENSP00000501555.1:n.*1743A=
ENST00000483302.6:n.2684A=
ENST00000498513.6:c.*910A= ENSP00000501637.1:n.*910A=
ENST00000674511.1:n.1618A=
ENST00000674516.1:c.*635A= ENSP00000502441.1:n.*635A=
ENST00000674621.1:n.1861-2257A=
ENST00000674771.1:c.*662A= ENSP00000502627.1:n.*662A=
ENST00000674784.1:c.*1079A= ENSP00000501837.1:n.*1079A=
ENST00000674970.1:c.*1793A= ENSP00000502493.1:n.*1793A=
ENST00000675012.1:n.1963A=
ENST00000675141.1:c.1920A= ENSP00000502420.1:p.Ser640=
ENST00000675198.1:n.1899A=
ENST00000675213.1:c.1974A= ENSP00000502218.1:p.Ser658=
ENST00000675224.1:c.*85A= ENSP00000501869.1:n.*85A=
ENST00000675253.1:c.*691A= ENSP00000502557.1:n.*691A=
ENST00000675445.1:c.*1691A= ENSP00000502253.1:n.*1691A=
ENST00000675448.1:c.2019A= ENSP00000502167.1:p.Ser673=
ENST00000675521.1:n.1929A=
ENST00000675572.1:c.1920A= ENSP00000501598.1:p.Ser640=
ENST00000675641.1:c.*761A= ENSP00000501845.1:n.*761A=
ENST00000675657.1:c.*632A= ENSP00000502002.1:n.*632A=
ENST00000675662.1:n.1814A=
ENST00000675789.1:c.1839A= ENSP00000501954.1:p.Ser613=
ENST00000675883.1:c.1938A= ENSP00000501592.1:p.Ser646=
ENST00000675945.1:c.*660A= ENSP00000501835.1:n.*660A=
ENST00000676014.1:c.1962A= ENSP00000502058.1:p.Ser654=
ENST00000676035.1:n.1681A=
ENST00000676106.1:n.2056A=
ENST00000676137.1:n.2049A=
ENST00000676170.1:c.2100A= ENSP00000502177.1:p.Ser700=
ENST00000676318.1:c.*2849A= ENSP00000502300.1:n.*2849A=
ENST00000676336.1:c.*632A= ENSP00000502686.1:n.*632A=
ENST00000676349.1:c.*1707A= ENSP00000502155.1:n.*1707A=
ENST00000676399.1:n.1922A=
ENST00000676409.1:n.2079A=
ENST00000300417.10:c.2019A= ENSP00000300417.6:p.Ser673=
ENST00000323301.8:c.2019A= ENSP00000322937.4:p.Ser673=
ENST00000373322.1:c.2019A= ENSP00000362419.1:p.Ser673=
ENST00000373324.8:c.1938A= ENSP00000362421.4:p.Ser646=
ENST00000483302.5:n.1241A=
NM_001005373.3:c.2019A= NP_001005373.1:p.Ser673=
NM_001005374.3:c.2019A= NP_001005374.1:p.Ser673=
NM_001190723.2:c.1938A= NP_001177652.1:p.Ser646=
NM_138361.5:c.2019A= , LRG_373t1:c.2019A= NP_612370.3:p.Ser673=
XM_006717316.2:c.1920A= XP_006717379.1:p.Ser640=
XM_006717316.4:c.1920A= XP_006717379.1:p.Ser640=
XM_017015283.1:c.2019A= XP_016870772.1:p.Ser673=
XM_017015284.2:c.1230A= XP_016870773.1:p.Ser410=
XR_001746415.2:n.2554A=
XR_929874.3:n.2378A=
NM_001190723.3:c.1938A= NP_001177652.1:p.Ser646=
NM_001005373.4:c.2019A= MANE Select NP_001005373.1:p.Ser673=
NM_001005374.4:c.2019A= NP_001005374.1:p.Ser673=
NM_001384142.1:c.2019A= NP_001371071.1:p.Ser673=
NM_001384143.1:c.1920A= NP_001371072.1:p.Ser640=
NM_001384144.1:c.1230A= NP_001371073.1:p.Ser410=
NR_168891.1:n.2548A=
NR_168892.1:n.2372A=