Canonical Allele Identifier: CA374934375

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127492844C>T , CM000671.2:g.127492844C>T	GRCh38
NC_000009.11:g.130255123C>T , CM000671.1:g.130255123C>T	GRCh37
NC_000009.10:g.129294944C>T	NCBI36
NG_032008.1:g.46359C>T , LRG_373:g.46359C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001005373.4:c.1546C>T MANE Select	NP_001005373.1:p.Gln516Ter
ENST00000300417.11:c.1546C>T MANE Select	ENSP00000300417.6:p.Gln516Ter
NM_001005373.3:c.1546C>T	NP_001005373.1:p.Gln516Ter
NM_001005374.3:c.1546C>T	NP_001005374.1:p.Gln516Ter
NM_001005374.4:c.1546C>T	NP_001005374.1:p.Gln516Ter
NM_001190723.2:c.1465C>T	NP_001177652.1:p.Gln489Ter
NM_001190723.3:c.1465C>T	NP_001177652.1:p.Gln489Ter
NM_001384142.1:c.1546C>T	NP_001371071.1:p.Gln516Ter
NM_001384143.1:c.1546C>T	NP_001371072.1:p.Gln516Ter
NM_001384144.1:c.757C>T	NP_001371073.1:p.Gln253Ter
NM_138361.5:c.1546C>T , LRG_373t1:c.1546C>T	NP_612370.3:p.Gln516Ter
NR_168891.1:n.2075C>T
NR_168892.1:n.1899C>T
ENST00000300417.10:c.1546C>T	ENSP00000300417.6:p.Gln516Ter
ENST00000323301.8:c.1546C>T	ENSP00000322937.4:p.Gln516Ter
ENST00000373322.1:c.1546C>T	ENSP00000362419.1:p.Gln516Ter
ENST00000373324.8:c.1465C>T	ENSP00000362421.4:p.Gln489Ter
ENST00000472068.1:n.538C>T
ENST00000472068.2:c.*1274C>T	ENSP00000501555.1:n.*1274C>T
ENST00000483302.5:n.768C>T
ENST00000483302.6:n.343C>T
ENST00000498513.6:c.*437C>T	ENSP00000501637.1:n.*437C>T
ENST00000674511.1:n.1298-3120C>T
ENST00000674516.1:c.1546C>T	ENSP00000502441.1:p.Gln516Ter
ENST00000674621.1:n.1596C>T
ENST00000674771.1:c.*288C>T	ENSP00000502627.1:n.*288C>T
ENST00000674784.1:c.*705C>T	ENSP00000501837.1:n.*705C>T
ENST00000674970.1:c.*1320C>T	ENSP00000502493.1:n.*1320C>T
ENST00000675012.1:n.1490C>T
ENST00000675141.1:c.1546C>T	ENSP00000502420.1:p.Gln516Ter
ENST00000675198.1:n.1426C>T
ENST00000675213.1:c.1501C>T	ENSP00000502218.1:p.Gln501Ter
ENST00000675224.1:c.1546C>T	ENSP00000501869.1:p.Gln516Ter
ENST00000675253.1:c.*317C>T	ENSP00000502557.1:n.*317C>T
ENST00000675445.1:c.*1218C>T	ENSP00000502253.1:n.*1218C>T
ENST00000675448.1:c.1546C>T	ENSP00000502167.1:p.Gln516Ter
ENST00000675521.1:n.1456C>T
ENST00000675572.1:c.1546C>T	ENSP00000501598.1:p.Gln516Ter
ENST00000675641.1:c.*288C>T	ENSP00000501845.1:n.*288C>T
ENST00000675657.1:c.*159C>T	ENSP00000502002.1:n.*159C>T
ENST00000675662.1:n.1341C>T
ENST00000675789.1:c.1465C>T	ENSP00000501954.1:p.Gln489Ter
ENST00000675883.1:c.1465C>T	ENSP00000501592.1:p.Gln489Ter
ENST00000675945.1:c.*368C>T	ENSP00000501835.1:n.*368C>T
ENST00000676014.1:c.1489C>T	ENSP00000502058.1:p.Gln497Ter
ENST00000676035.1:n.1307C>T
ENST00000676106.1:n.1351C>T
ENST00000676137.1:n.1576C>T
ENST00000676170.1:c.1627C>T	ENSP00000502177.1:p.Gln543Ter
ENST00000676318.1:c.*288C>T	ENSP00000502300.1:n.*288C>T
ENST00000676336.1:c.*159C>T	ENSP00000502686.1:n.*159C>T
ENST00000676349.1:c.*1234C>T	ENSP00000502155.1:n.*1234C>T
ENST00000676399.1:n.1449C>T
ENST00000676409.1:n.1606C>T
XM_006717316.2:c.1546C>T	XP_006717379.1:p.Gln516Ter
XM_006717316.4:c.1546C>T	XP_006717379.1:p.Gln516Ter
XM_017015283.1:c.1546C>T	XP_016870772.1:p.Gln516Ter
XM_017015284.2:c.757C>T	XP_016870773.1:p.Gln253Ter
XR_001746415.2:n.2081C>T
XR_929874.3:n.1905C>T