Canonical Allele Identifier: CA199849239

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127483005C>T , CM000671.2:g.127483005C>T	GRCh38
NC_000009.11:g.130245284C>T , CM000671.1:g.130245284C>T	GRCh37
NC_000009.10:g.129285105C>T	NCBI36
NG_032008.1:g.36520C>T , LRG_373:g.36520C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001005373.4:c.1144C>T MANE Select	NP_001005373.1:p.Arg382Ter
ENST00000300417.11:c.1144C>T MANE Select	ENSP00000300417.6:p.Arg382Ter
NM_001005373.3:c.1144C>T	NP_001005373.1:p.Arg382Ter
NM_001005374.3:c.1144C>T	NP_001005374.1:p.Arg382Ter
NM_001005374.4:c.1144C>T	NP_001005374.1:p.Arg382Ter
NM_001190723.2:c.1144C>T	NP_001177652.1:p.Arg382Ter
NM_001190723.3:c.1144C>T	NP_001177652.1:p.Arg382Ter
NM_001384142.1:c.1144C>T	NP_001371071.1:p.Arg382Ter
NM_001384143.1:c.1144C>T	NP_001371072.1:p.Arg382Ter
NM_001384144.1:c.355C>T	NP_001371073.1:p.Arg119Ter
NM_138361.5:c.1144C>T , LRG_373t1:c.1144C>T	NP_612370.3:p.Arg382Ter
NR_168891.1:n.1492C>T
NR_168892.1:n.1492C>T
ENST00000300417.10:c.1144C>T	ENSP00000300417.6:p.Arg382Ter
ENST00000323301.8:c.1144C>T	ENSP00000322937.4:p.Arg382Ter
ENST00000373322.1:c.1144C>T	ENSP00000362419.1:p.Arg382Ter
ENST00000373324.8:c.1144C>T	ENSP00000362421.4:p.Arg382Ter
ENST00000472068.1:n.131C>T
ENST00000472068.2:c.*867C>T	ENSP00000501555.1:n.*867C>T
ENST00000483302.5:n.361C>T
ENST00000498513.5:n.397C>T
ENST00000498513.6:c.397C>T	ENSP00000501637.1:p.Arg133Ter
ENST00000674511.1:n.1019C>T
ENST00000674516.1:c.1144C>T	ENSP00000502441.1:p.Arg382Ter
ENST00000674621.1:n.1050C>T
ENST00000674771.1:c.1144C>T	ENSP00000502627.1:p.Arg382Ter
ENST00000674784.1:c.*318+1778C>T	ENSP00000501837.1:n.*318+1778C>T
ENST00000674970.1:c.*918C>T	ENSP00000502493.1:n.*918C>T
ENST00000675012.1:n.1024C>T
ENST00000675141.1:c.1144C>T	ENSP00000502420.1:p.Arg382Ter
ENST00000675198.1:n.1046C>T
ENST00000675213.1:c.1099C>T	ENSP00000502218.1:p.Arg367Ter
ENST00000675224.1:c.1144C>T	ENSP00000501869.1:p.Arg382Ter
ENST00000675253.1:c.1144C>T	ENSP00000502557.1:p.Arg382Ter
ENST00000675445.1:c.*816C>T	ENSP00000502253.1:n.*816C>T
ENST00000675448.1:c.1144C>T	ENSP00000502167.1:p.Arg382Ter
ENST00000675521.1:n.996C>T
ENST00000675572.1:c.1144C>T	ENSP00000501598.1:p.Arg382Ter
ENST00000675641.1:c.1144C>T	ENSP00000501845.1:p.Arg382Ter
ENST00000675657.1:c.1144C>T	ENSP00000502002.1:p.Arg382Ter
ENST00000675662.1:n.1037C>T
ENST00000675789.1:c.1144C>T	ENSP00000501954.1:p.Arg382Ter
ENST00000675883.1:c.1144C>T	ENSP00000501592.1:p.Arg382Ter
ENST00000675945.1:c.1144C>T	ENSP00000501835.1:p.Arg382Ter
ENST00000676014.1:c.1087C>T	ENSP00000502058.1:p.Arg363Ter
ENST00000676035.1:n.905C>T
ENST00000676106.1:n.949C>T
ENST00000676137.1:n.1035C>T
ENST00000676170.1:c.1225C>T	ENSP00000502177.1:p.Arg409Ter
ENST00000676318.1:c.1144C>T	ENSP00000502300.1:p.Arg382Ter
ENST00000676336.1:c.922C>T	ENSP00000502686.1:p.Arg308Ter
ENST00000676349.1:c.*913C>T	ENSP00000502155.1:n.*913C>T
ENST00000676399.1:n.1042C>T
ENST00000676409.1:n.1023C>T
XM_006717316.2:c.1144C>T	XP_006717379.1:p.Arg382Ter
XM_006717316.4:c.1144C>T	XP_006717379.1:p.Arg382Ter
XM_017015283.1:c.1144C>T	XP_016870772.1:p.Arg382Ter
XM_017015284.2:c.355C>T	XP_016870773.1:p.Arg119Ter
XR_001746415.2:n.1498C>T
XR_929874.1:n.1516C>T
XR_929874.3:n.1498C>T