Canonical Allele Identifier: CA2839975185

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127485799dup , CM000671.2:g.127485799dup	GRCh38
NC_000009.11:g.130248078dup , CM000671.1:g.130248078dup	GRCh37
NC_000009.10:g.129287899dup	NCBI36
NG_032008.1:g.39314dup , LRG_373:g.39314dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1223dup MANE Select	ENSP00000300417.6:p.Gln409SerfsTer18
ENST00000472068.2:c.*946dup	ENSP00000501555.1:n.*946dup
ENST00000498513.6:c.476dup	ENSP00000501637.1:p.Gln160SerfsTer?
ENST00000674511.1:n.1098dup
ENST00000674516.1:c.1223dup	ENSP00000502441.1:p.Gln409SerfsTer18
ENST00000674621.1:n.1129dup
ENST00000674771.1:c.1223dup	ENSP00000502627.1:p.Gln409SerfsTer?
ENST00000674784.1:c.*382dup	ENSP00000501837.1:n.*382dup
ENST00000674970.1:c.*997dup	ENSP00000502493.1:n.*997dup
ENST00000675012.1:n.1103dup
ENST00000675141.1:c.1223dup	ENSP00000502420.1:p.Gln409SerfsTer18
ENST00000675198.1:n.1125dup
ENST00000675213.1:c.1178dup	ENSP00000502218.1:p.Gln394SerfsTer18
ENST00000675224.1:c.1223dup	ENSP00000501869.1:p.Gln409SerfsTer18
ENST00000675253.1:c.1223dup	ENSP00000502557.1:p.Gln409SerfsTer26
ENST00000675445.1:c.*895dup	ENSP00000502253.1:n.*895dup
ENST00000675448.1:c.1223dup	ENSP00000502167.1:p.Gln409SerfsTer18
ENST00000675521.1:n.1075dup
ENST00000675572.1:c.1223dup	ENSP00000501598.1:p.Gln409SerfsTer18
ENST00000675641.1:c.1223dup	ENSP00000501845.1:p.Gln409SerfsTer?
ENST00000675657.1:c.1223dup	ENSP00000502002.1:p.Gln409SerfsTer?
ENST00000675662.1:n.1082+34dup
ENST00000675789.1:c.1223dup	ENSP00000501954.1:p.Gln409SerfsTer18
ENST00000675883.1:c.1223dup	ENSP00000501592.1:p.Gln409SerfsTer18
ENST00000675945.1:c.1223dup	ENSP00000501835.1:p.Gln409SerfsTer?
ENST00000676014.1:c.1166dup	ENSP00000502058.1:p.Gln390SerfsTer18
ENST00000676035.1:n.984dup
ENST00000676106.1:n.1028dup
ENST00000676137.1:n.1114dup
ENST00000676170.1:c.1304dup	ENSP00000502177.1:p.Gln436SerfsTer18
ENST00000676318.1:c.1223dup	ENSP00000502300.1:p.Gln409SerfsTer?
ENST00000676336.1:c.1001dup	ENSP00000502686.1:p.Gln335SerfsTer?
ENST00000676349.1:c.*992dup	ENSP00000502155.1:n.*992dup
ENST00000676399.1:n.1121dup
ENST00000676409.1:n.1102dup
ENST00000300417.10:c.1223dup	ENSP00000300417.6:p.Gln409SerfsTer18
ENST00000323301.8:c.1223dup	ENSP00000322937.4:p.Gln409SerfsTer18
ENST00000373322.1:c.1223dup	ENSP00000362419.1:p.Gln409SerfsTer18
ENST00000373324.8:c.1223dup	ENSP00000362421.4:p.Gln409SerfsTer18
ENST00000472068.1:n.210dup
ENST00000483302.5:n.440dup
ENST00000498513.5:n.476dup
NM_001005373.3:c.1223dup	NP_001005373.1:p.Gln409SerfsTer18
NM_001005374.3:c.1223dup	NP_001005374.1:p.Gln409SerfsTer18
NM_001190723.2:c.1223dup	NP_001177652.1:p.Gln409SerfsTer18
NM_138361.5:c.1223dup , LRG_373t1:c.1223dup	NP_612370.3:p.Gln409SerfsTer18
XM_006717316.2:c.1223dup	XP_006717379.1:p.Gln409SerfsTer18
XR_929874.1:n.1595dup
XM_006717316.4:c.1223dup	XP_006717379.1:p.Gln409SerfsTer18
XM_017015283.1:c.1223dup	XP_016870772.1:p.Gln409SerfsTer18
XM_017015284.2:c.434dup	XP_016870773.1:p.Gln146SerfsTer18
XR_001746415.2:n.1577dup
XR_929874.3:n.1577dup
NM_001190723.3:c.1223dup	NP_001177652.1:p.Gln409SerfsTer18
NM_001005373.4:c.1223dup MANE Select	NP_001005373.1:p.Gln409SerfsTer18
NM_001005374.4:c.1223dup	NP_001005374.1:p.Gln409SerfsTer18
NM_001384142.1:c.1223dup	NP_001371071.1:p.Gln409SerfsTer18
NM_001384143.1:c.1223dup	NP_001371072.1:p.Gln409SerfsTer18
NM_001384144.1:c.434dup	NP_001371073.1:p.Gln146SerfsTer18
NR_168891.1:n.1571dup
NR_168892.1:n.1571dup