Canonical Allele Identifier: CA1879828519
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501035C= , CM000671.2:g.127501035C= GRCh38
NC_000009.11:g.130263314C= , CM000671.1:g.130263314C= GRCh37
NC_000009.10:g.129303135C= NCBI36
NG_032008.1:g.54550C= , LRG_373:g.54550C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1938C= MANE Select ENSP00000300417.6:p.Val646=
ENST00000472068.2:c.*1662C= ENSP00000501555.1:n.*1662C=
ENST00000483302.6:n.2603C=
ENST00000498513.6:c.*829C= ENSP00000501637.1:n.*829C=
ENST00000674511.1:n.1537C=
ENST00000674516.1:c.*554C= ENSP00000502441.1:n.*554C=
ENST00000674621.1:n.1861-2338C=
ENST00000674771.1:c.*581C= ENSP00000502627.1:n.*581C=
ENST00000674784.1:c.*998C= ENSP00000501837.1:n.*998C=
ENST00000674970.1:c.*1712C= ENSP00000502493.1:n.*1712C=
ENST00000675012.1:n.1882C=
ENST00000675141.1:c.1839C= ENSP00000502420.1:p.Val613=
ENST00000675198.1:n.1818C=
ENST00000675213.1:c.1893C= ENSP00000502218.1:p.Val631=
ENST00000675224.1:c.*4C= ENSP00000501869.1:n.*4C=
ENST00000675253.1:c.*610C= ENSP00000502557.1:n.*610C=
ENST00000675445.1:c.*1610C= ENSP00000502253.1:n.*1610C=
ENST00000675448.1:c.1938C= ENSP00000502167.1:p.Val646=
ENST00000675521.1:n.1848C=
ENST00000675572.1:c.1839C= ENSP00000501598.1:p.Val613=
ENST00000675641.1:c.*680C= ENSP00000501845.1:n.*680C=
ENST00000675657.1:c.*551C= ENSP00000502002.1:n.*551C=
ENST00000675662.1:n.1733C=
ENST00000675789.1:c.1758C= ENSP00000501954.1:p.Val586=
ENST00000675883.1:c.1857C= ENSP00000501592.1:p.Val619=
ENST00000675945.1:c.*579C= ENSP00000501835.1:n.*579C=
ENST00000676014.1:c.1881C= ENSP00000502058.1:p.Val627=
ENST00000676035.1:n.1600C=
ENST00000676106.1:n.1975C=
ENST00000676137.1:n.1968C=
ENST00000676170.1:c.2019C= ENSP00000502177.1:p.Val673=
ENST00000676318.1:c.*2768C= ENSP00000502300.1:n.*2768C=
ENST00000676336.1:c.*551C= ENSP00000502686.1:n.*551C=
ENST00000676349.1:c.*1626C= ENSP00000502155.1:n.*1626C=
ENST00000676399.1:n.1841C=
ENST00000676409.1:n.1998C=
ENST00000300417.10:c.1938C= ENSP00000300417.6:p.Val646=
ENST00000323301.8:c.1938C= ENSP00000322937.4:p.Val646=
ENST00000373322.1:c.1938C= ENSP00000362419.1:p.Val646=
ENST00000373324.8:c.1857C= ENSP00000362421.4:p.Val619=
ENST00000472068.1:n.831C=
ENST00000483302.5:n.1160C=
NM_001005373.3:c.1938C= NP_001005373.1:p.Val646=
NM_001005374.3:c.1938C= NP_001005374.1:p.Val646=
NM_001190723.2:c.1857C= NP_001177652.1:p.Val619=
NM_138361.5:c.1938C= , LRG_373t1:c.1938C= NP_612370.3:p.Val646=
XM_006717316.2:c.1839C= XP_006717379.1:p.Val613=
XM_006717316.4:c.1839C= XP_006717379.1:p.Val613=
XM_017015283.1:c.1938C= XP_016870772.1:p.Val646=
XM_017015284.2:c.1149C= XP_016870773.1:p.Val383=
XR_001746415.2:n.2473C=
XR_929874.3:n.2297C=
NM_001190723.3:c.1857C= NP_001177652.1:p.Val619=
NM_001005373.4:c.1938C= MANE Select NP_001005373.1:p.Val646=
NM_001005374.4:c.1938C= NP_001005374.1:p.Val646=
NM_001384142.1:c.1938C= NP_001371071.1:p.Val646=
NM_001384143.1:c.1839C= NP_001371072.1:p.Val613=
NM_001384144.1:c.1149C= NP_001371073.1:p.Val383=
NR_168891.1:n.2467C=
NR_168892.1:n.2291C=