Canonical Allele Identifier: CA1879828601
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501052C= , CM000671.2:g.127501052C= GRCh38
NC_000009.11:g.130263331C= , CM000671.1:g.130263331C= GRCh37
NC_000009.10:g.129303152C= NCBI36
NG_032008.1:g.54567C= , LRG_373:g.54567C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1955C= MANE Select ENSP00000300417.6:p.Pro652=
ENST00000472068.2:c.*1679C= ENSP00000501555.1:n.*1679C=
ENST00000483302.6:n.2620C=
ENST00000498513.6:c.*846C= ENSP00000501637.1:n.*846C=
ENST00000674511.1:n.1554C=
ENST00000674516.1:c.*571C= ENSP00000502441.1:n.*571C=
ENST00000674621.1:n.1861-2321C=
ENST00000674771.1:c.*598C= ENSP00000502627.1:n.*598C=
ENST00000674784.1:c.*1015C= ENSP00000501837.1:n.*1015C=
ENST00000674970.1:c.*1729C= ENSP00000502493.1:n.*1729C=
ENST00000675012.1:n.1899C=
ENST00000675141.1:c.1856C= ENSP00000502420.1:p.Pro619=
ENST00000675198.1:n.1835C=
ENST00000675213.1:c.1910C= ENSP00000502218.1:p.Pro637=
ENST00000675224.1:c.*21C= ENSP00000501869.1:n.*21C=
ENST00000675253.1:c.*627C= ENSP00000502557.1:n.*627C=
ENST00000675445.1:c.*1627C= ENSP00000502253.1:n.*1627C=
ENST00000675448.1:c.1955C= ENSP00000502167.1:p.Pro652=
ENST00000675521.1:n.1865C=
ENST00000675572.1:c.1856C= ENSP00000501598.1:p.Pro619=
ENST00000675641.1:c.*697C= ENSP00000501845.1:n.*697C=
ENST00000675657.1:c.*568C= ENSP00000502002.1:n.*568C=
ENST00000675662.1:n.1750C=
ENST00000675789.1:c.1775C= ENSP00000501954.1:p.Pro592=
ENST00000675883.1:c.1874C= ENSP00000501592.1:p.Pro625=
ENST00000675945.1:c.*596C= ENSP00000501835.1:n.*596C=
ENST00000676014.1:c.1898C= ENSP00000502058.1:p.Pro633=
ENST00000676035.1:n.1617C=
ENST00000676106.1:n.1992C=
ENST00000676137.1:n.1985C=
ENST00000676170.1:c.2036C= ENSP00000502177.1:p.Pro679=
ENST00000676318.1:c.*2785C= ENSP00000502300.1:n.*2785C=
ENST00000676336.1:c.*568C= ENSP00000502686.1:n.*568C=
ENST00000676349.1:c.*1643C= ENSP00000502155.1:n.*1643C=
ENST00000676399.1:n.1858C=
ENST00000676409.1:n.2015C=
ENST00000300417.10:c.1955C= ENSP00000300417.6:p.Pro652=
ENST00000323301.8:c.1955C= ENSP00000322937.4:p.Pro652=
ENST00000373322.1:c.1955C= ENSP00000362419.1:p.Pro652=
ENST00000373324.8:c.1874C= ENSP00000362421.4:p.Pro625=
ENST00000472068.1:n.848C=
ENST00000483302.5:n.1177C=
NM_001005373.3:c.1955C= NP_001005373.1:p.Pro652=
NM_001005374.3:c.1955C= NP_001005374.1:p.Pro652=
NM_001190723.2:c.1874C= NP_001177652.1:p.Pro625=
NM_138361.5:c.1955C= , LRG_373t1:c.1955C= NP_612370.3:p.Pro652=
XM_006717316.2:c.1856C= XP_006717379.1:p.Pro619=
XM_006717316.4:c.1856C= XP_006717379.1:p.Pro619=
XM_017015283.1:c.1955C= XP_016870772.1:p.Pro652=
XM_017015284.2:c.1166C= XP_016870773.1:p.Pro389=
XR_001746415.2:n.2490C=
XR_929874.3:n.2314C=
NM_001190723.3:c.1874C= NP_001177652.1:p.Pro625=
NM_001005373.4:c.1955C= MANE Select NP_001005373.1:p.Pro652=
NM_001005374.4:c.1955C= NP_001005374.1:p.Pro652=
NM_001384142.1:c.1955C= NP_001371071.1:p.Pro652=
NM_001384143.1:c.1856C= NP_001371072.1:p.Pro619=
NM_001384144.1:c.1166C= NP_001371073.1:p.Pro389=
NR_168891.1:n.2484C=
NR_168892.1:n.2308C=