Canonical Allele Identifier: CA2573332141

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501108del , CM000671.2:g.127501108del	GRCh38
NC_000009.11:g.130263387del , CM000671.1:g.130263387del	GRCh37
NC_000009.10:g.129303208del	NCBI36
NG_032008.1:g.54623del , LRG_373:g.54623del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2011del MANE Select	ENSP00000300417.6:p.Gln671ArgfsTer15
ENST00000472068.2:c.*1735del	ENSP00000501555.1:n.*1735del
ENST00000483302.6:n.2676del
ENST00000498513.6:c.*902del	ENSP00000501637.1:n.*902del
ENST00000674511.1:n.1610del
ENST00000674516.1:c.*627del	ENSP00000502441.1:n.*627del
ENST00000674621.1:n.1861-2265del
ENST00000674771.1:c.*654del	ENSP00000502627.1:n.*654del
ENST00000674784.1:c.*1071del	ENSP00000501837.1:n.*1071del
ENST00000674970.1:c.*1785del	ENSP00000502493.1:n.*1785del
ENST00000675012.1:n.1955del
ENST00000675141.1:c.1912del	ENSP00000502420.1:p.Gln638ArgfsTer15
ENST00000675198.1:n.1891del
ENST00000675213.1:c.1966del	ENSP00000502218.1:p.Gln656ArgfsTer15
ENST00000675224.1:c.*77del	ENSP00000501869.1:n.*77del
ENST00000675253.1:c.*683del	ENSP00000502557.1:n.*683del
ENST00000675445.1:c.*1683del	ENSP00000502253.1:n.*1683del
ENST00000675448.1:c.2011del	ENSP00000502167.1:p.Gln671ArgfsTer15
ENST00000675521.1:n.1921del
ENST00000675572.1:c.1912del	ENSP00000501598.1:p.Gln638ArgfsTer15
ENST00000675641.1:c.*753del	ENSP00000501845.1:n.*753del
ENST00000675657.1:c.*624del	ENSP00000502002.1:n.*624del
ENST00000675662.1:n.1806del
ENST00000675789.1:c.1831del	ENSP00000501954.1:p.Gln611ArgfsTer15
ENST00000675883.1:c.1930del	ENSP00000501592.1:p.Gln644ArgfsTer15
ENST00000675945.1:c.*652del	ENSP00000501835.1:n.*652del
ENST00000676014.1:c.1954del	ENSP00000502058.1:p.Gln652ArgfsTer15
ENST00000676035.1:n.1673del
ENST00000676106.1:n.2048del
ENST00000676137.1:n.2041del
ENST00000676170.1:c.2092del	ENSP00000502177.1:p.Gln698ArgfsTer15
ENST00000676318.1:c.*2841del	ENSP00000502300.1:n.*2841del
ENST00000676336.1:c.*624del	ENSP00000502686.1:n.*624del
ENST00000676349.1:c.*1699del	ENSP00000502155.1:n.*1699del
ENST00000676399.1:n.1914del
ENST00000676409.1:n.2071del
ENST00000300417.10:c.2011del	ENSP00000300417.6:p.Gln671ArgfsTer15
ENST00000323301.8:c.2011del	ENSP00000322937.4:p.Gln671ArgfsTer15
ENST00000373322.1:c.2011del	ENSP00000362419.1:p.Gln671ArgfsTer15
ENST00000373324.8:c.1930del	ENSP00000362421.4:p.Gln644ArgfsTer15
ENST00000483302.5:n.1233del
NM_001005373.3:c.2011del	NP_001005373.1:p.Gln671ArgfsTer15
NM_001005374.3:c.2011del	NP_001005374.1:p.Gln671ArgfsTer15
NM_001190723.2:c.1930del	NP_001177652.1:p.Gln644ArgfsTer15
NM_138361.5:c.2011del , LRG_373t1:c.2011del	NP_612370.3:p.Gln671ArgfsTer15
XM_006717316.2:c.1912del	XP_006717379.1:p.Gln638ArgfsTer15
XM_006717316.4:c.1912del	XP_006717379.1:p.Gln638ArgfsTer15
XM_017015283.1:c.2011del	XP_016870772.1:p.Gln671ArgfsTer15
XM_017015284.2:c.1222del	XP_016870773.1:p.Gln408ArgfsTer15
XR_001746415.2:n.2546del
XR_929874.3:n.2370del
NM_001190723.3:c.1930del	NP_001177652.1:p.Gln644ArgfsTer15
NM_001005373.4:c.2011del MANE Select	NP_001005373.1:p.Gln671ArgfsTer15
NM_001005374.4:c.2011del	NP_001005374.1:p.Gln671ArgfsTer15
NM_001384142.1:c.2011del	NP_001371071.1:p.Gln671ArgfsTer15
NM_001384143.1:c.1912del	NP_001371072.1:p.Gln638ArgfsTer15
NM_001384144.1:c.1222del	NP_001371073.1:p.Gln408ArgfsTer15
NR_168891.1:n.2540del
NR_168892.1:n.2364del