Canonical Allele Identifier: CA1879828770
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501106T= , CM000671.2:g.127501106T= GRCh38
NC_000009.11:g.130263385T= , CM000671.1:g.130263385T= GRCh37
NC_000009.10:g.129303206T= NCBI36
NG_032008.1:g.54621T= , LRG_373:g.54621T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.2009T= MANE Select ENSP00000300417.6:p.Val670=
ENST00000472068.2:c.*1733T= ENSP00000501555.1:n.*1733T=
ENST00000483302.6:n.2674T=
ENST00000498513.6:c.*900T= ENSP00000501637.1:n.*900T=
ENST00000674511.1:n.1608T=
ENST00000674516.1:c.*625T= ENSP00000502441.1:n.*625T=
ENST00000674621.1:n.1861-2267T=
ENST00000674771.1:c.*652T= ENSP00000502627.1:n.*652T=
ENST00000674784.1:c.*1069T= ENSP00000501837.1:n.*1069T=
ENST00000674970.1:c.*1783T= ENSP00000502493.1:n.*1783T=
ENST00000675012.1:n.1953T=
ENST00000675141.1:c.1910T= ENSP00000502420.1:p.Val637=
ENST00000675198.1:n.1889T=
ENST00000675213.1:c.1964T= ENSP00000502218.1:p.Val655=
ENST00000675224.1:c.*75T= ENSP00000501869.1:n.*75T=
ENST00000675253.1:c.*681T= ENSP00000502557.1:n.*681T=
ENST00000675445.1:c.*1681T= ENSP00000502253.1:n.*1681T=
ENST00000675448.1:c.2009T= ENSP00000502167.1:p.Val670=
ENST00000675521.1:n.1919T=
ENST00000675572.1:c.1910T= ENSP00000501598.1:p.Val637=
ENST00000675641.1:c.*751T= ENSP00000501845.1:n.*751T=
ENST00000675657.1:c.*622T= ENSP00000502002.1:n.*622T=
ENST00000675662.1:n.1804T=
ENST00000675789.1:c.1829T= ENSP00000501954.1:p.Val610=
ENST00000675883.1:c.1928T= ENSP00000501592.1:p.Val643=
ENST00000675945.1:c.*650T= ENSP00000501835.1:n.*650T=
ENST00000676014.1:c.1952T= ENSP00000502058.1:p.Val651=
ENST00000676035.1:n.1671T=
ENST00000676106.1:n.2046T=
ENST00000676137.1:n.2039T=
ENST00000676170.1:c.2090T= ENSP00000502177.1:p.Val697=
ENST00000676318.1:c.*2839T= ENSP00000502300.1:n.*2839T=
ENST00000676336.1:c.*622T= ENSP00000502686.1:n.*622T=
ENST00000676349.1:c.*1697T= ENSP00000502155.1:n.*1697T=
ENST00000676399.1:n.1912T=
ENST00000676409.1:n.2069T=
ENST00000300417.10:c.2009T= ENSP00000300417.6:p.Val670=
ENST00000323301.8:c.2009T= ENSP00000322937.4:p.Val670=
ENST00000373322.1:c.2009T= ENSP00000362419.1:p.Val670=
ENST00000373324.8:c.1928T= ENSP00000362421.4:p.Val643=
ENST00000483302.5:n.1231T=
NM_001005373.3:c.2009T= NP_001005373.1:p.Val670=
NM_001005374.3:c.2009T= NP_001005374.1:p.Val670=
NM_001190723.2:c.1928T= NP_001177652.1:p.Val643=
NM_138361.5:c.2009T= , LRG_373t1:c.2009T= NP_612370.3:p.Val670=
XM_006717316.2:c.1910T= XP_006717379.1:p.Val637=
XM_006717316.4:c.1910T= XP_006717379.1:p.Val637=
XM_017015283.1:c.2009T= XP_016870772.1:p.Val670=
XM_017015284.2:c.1220T= XP_016870773.1:p.Val407=
XR_001746415.2:n.2544T=
XR_929874.3:n.2368T=
NM_001190723.3:c.1928T= NP_001177652.1:p.Val643=
NM_001005373.4:c.2009T= MANE Select NP_001005373.1:p.Val670=
NM_001005374.4:c.2009T= NP_001005374.1:p.Val670=
NM_001384142.1:c.2009T= NP_001371071.1:p.Val670=
NM_001384143.1:c.1910T= NP_001371072.1:p.Val637=
NM_001384144.1:c.1220T= NP_001371073.1:p.Val407=
NR_168891.1:n.2538T=
NR_168892.1:n.2362T=