Canonical Allele Identifier: CA1879828441
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127500998T= , CM000671.2:g.127500998T= GRCh38
NC_000009.11:g.130263277T= , CM000671.1:g.130263277T= GRCh37
NC_000009.10:g.129303098T= NCBI36
NG_032008.1:g.54513T= , LRG_373:g.54513T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1913-12T= MANE Select ENSP00000300417.6:n.1913-12T=
ENST00000472068.2:c.*1637-12T= ENSP00000501555.1:n.*1637-12T=
ENST00000483302.6:n.2578-12T=
ENST00000498513.6:c.*804-12T= ENSP00000501637.1:n.*804-12T=
ENST00000674511.1:n.1512-12T=
ENST00000674516.1:c.*529-12T= ENSP00000502441.1:n.*529-12T=
ENST00000674621.1:n.1861-2375T=
ENST00000674771.1:c.*556-12T= ENSP00000502627.1:n.*556-12T=
ENST00000674784.1:c.*973-12T= ENSP00000501837.1:n.*973-12T=
ENST00000674970.1:c.*1687-12T= ENSP00000502493.1:n.*1687-12T=
ENST00000675012.1:n.1857-12T=
ENST00000675141.1:c.1814-12T= ENSP00000502420.1:n.1814-12T=
ENST00000675198.1:n.1793-12T=
ENST00000675213.1:c.1868-12T= ENSP00000502218.1:n.1868-12T=
ENST00000675224.1:c.1941-12T= ENSP00000501869.1:n.1941-12T=
ENST00000675253.1:c.*585-12T= ENSP00000502557.1:n.*585-12T=
ENST00000675445.1:c.*1585-12T= ENSP00000502253.1:n.*1585-12T=
ENST00000675448.1:c.1913-12T= ENSP00000502167.1:n.1913-12T=
ENST00000675521.1:n.1823-12T=
ENST00000675572.1:c.1814-12T= ENSP00000501598.1:n.1814-12T=
ENST00000675641.1:c.*655-12T= ENSP00000501845.1:n.*655-12T=
ENST00000675657.1:c.*526-12T= ENSP00000502002.1:n.*526-12T=
ENST00000675662.1:n.1708-12T=
ENST00000675789.1:c.1733-12T= ENSP00000501954.1:n.1733-12T=
ENST00000675883.1:c.1832-12T= ENSP00000501592.1:n.1832-12T=
ENST00000675945.1:c.*554-12T= ENSP00000501835.1:n.*554-12T=
ENST00000676014.1:c.1856-12T= ENSP00000502058.1:n.1856-12T=
ENST00000676035.1:n.1575-12T=
ENST00000676106.1:n.1950-12T=
ENST00000676137.1:n.1943-12T=
ENST00000676170.1:c.1994-12T= ENSP00000502177.1:n.1994-12T=
ENST00000676318.1:c.*2743-12T= ENSP00000502300.1:n.*2743-12T=
ENST00000676336.1:c.*526-12T= ENSP00000502686.1:n.*526-12T=
ENST00000676349.1:c.*1601-12T= ENSP00000502155.1:n.*1601-12T=
ENST00000676399.1:n.1816-12T=
ENST00000676409.1:n.1973-12T=
ENST00000300417.10:c.1913-12T= ENSP00000300417.6:n.1913-12T=
ENST00000323301.8:c.1913-12T= ENSP00000322937.4:n.1913-12T=
ENST00000373322.1:c.1913-12T= ENSP00000362419.1:n.1913-12T=
ENST00000373324.8:c.1832-12T= ENSP00000362421.4:n.1832-12T=
ENST00000472068.1:n.806-12T=
ENST00000483302.5:n.1135-12T=
NM_001005373.3:c.1913-12T= NP_001005373.1:n.1913-12T=
NM_001005374.3:c.1913-12T= NP_001005374.1:n.1913-12T=
NM_001190723.2:c.1832-12T= NP_001177652.1:n.1832-12T=
NM_138361.5:c.1913-12T= , LRG_373t1:c.1913-12T= NP_612370.3:n.1913-12T=
XM_006717316.2:c.1814-12T= XP_006717379.1:n.1814-12T=
XM_006717316.4:c.1814-12T= XP_006717379.1:n.1814-12T=
XM_017015283.1:c.1913-12T= XP_016870772.1:n.1913-12T=
XM_017015284.2:c.1124-12T= XP_016870773.1:n.1124-12T=
XR_001746415.2:n.2448-12T=
XR_929874.3:n.2272-12T=
NM_001190723.3:c.1832-12T= NP_001177652.1:n.1832-12T=
NM_001005373.4:c.1913-12T= MANE Select NP_001005373.1:n.1913-12T=
NM_001005374.4:c.1913-12T= NP_001005374.1:n.1913-12T=
NM_001384142.1:c.1913-12T= NP_001371071.1:n.1913-12T=
NM_001384143.1:c.1814-12T= NP_001371072.1:n.1814-12T=
NM_001384144.1:c.1124-12T= NP_001371073.1:n.1124-12T=
NR_168891.1:n.2442-12T=
NR_168892.1:n.2266-12T=