Canonical Allele Identifier: CA374938292

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263381G>C (hg19) ; chr9:g.127501102G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501102G>C , CM000671.2:g.127501102G>C	GRCh38
NC_000009.11:g.130263381G>C , CM000671.1:g.130263381G>C	GRCh37
NC_000009.10:g.129303202G>C	NCBI36
NG_032008.1:g.54617G>C , LRG_373:g.54617G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2005G>C MANE Select	ENSP00000300417.6:p.Glu669Gln
ENST00000472068.2:c.*1729G>C	ENSP00000501555.1:n.*1729G>C
ENST00000483302.6:n.2670G>C
ENST00000498513.6:c.*896G>C	ENSP00000501637.1:n.*896G>C
ENST00000674511.1:n.1604G>C
ENST00000674516.1:c.*621G>C	ENSP00000502441.1:n.*621G>C
ENST00000674621.1:n.1861-2271G>C
ENST00000674771.1:c.*648G>C	ENSP00000502627.1:n.*648G>C
ENST00000674784.1:c.*1065G>C	ENSP00000501837.1:n.*1065G>C
ENST00000674970.1:c.*1779G>C	ENSP00000502493.1:n.*1779G>C
ENST00000675012.1:n.1949G>C
ENST00000675141.1:c.1906G>C	ENSP00000502420.1:p.Glu636Gln
ENST00000675198.1:n.1885G>C
ENST00000675213.1:c.1960G>C	ENSP00000502218.1:p.Glu654Gln
ENST00000675224.1:c.*71G>C	ENSP00000501869.1:n.*71G>C
ENST00000675253.1:c.*677G>C	ENSP00000502557.1:n.*677G>C
ENST00000675445.1:c.*1677G>C	ENSP00000502253.1:n.*1677G>C
ENST00000675448.1:c.2005G>C	ENSP00000502167.1:p.Glu669Gln
ENST00000675521.1:n.1915G>C
ENST00000675572.1:c.1906G>C	ENSP00000501598.1:p.Glu636Gln
ENST00000675641.1:c.*747G>C	ENSP00000501845.1:n.*747G>C
ENST00000675657.1:c.*618G>C	ENSP00000502002.1:n.*618G>C
ENST00000675662.1:n.1800G>C
ENST00000675789.1:c.1825G>C	ENSP00000501954.1:p.Glu609Gln
ENST00000675883.1:c.1924G>C	ENSP00000501592.1:p.Glu642Gln
ENST00000675945.1:c.*646G>C	ENSP00000501835.1:n.*646G>C
ENST00000676014.1:c.1948G>C	ENSP00000502058.1:p.Glu650Gln
ENST00000676035.1:n.1667G>C
ENST00000676106.1:n.2042G>C
ENST00000676137.1:n.2035G>C
ENST00000676170.1:c.2086G>C	ENSP00000502177.1:p.Glu696Gln
ENST00000676318.1:c.*2835G>C	ENSP00000502300.1:n.*2835G>C
ENST00000676336.1:c.*618G>C	ENSP00000502686.1:n.*618G>C
ENST00000676349.1:c.*1693G>C	ENSP00000502155.1:n.*1693G>C
ENST00000676399.1:n.1908G>C
ENST00000676409.1:n.2065G>C
ENST00000300417.10:c.2005G>C	ENSP00000300417.6:p.Glu669Gln
ENST00000323301.8:c.2005G>C	ENSP00000322937.4:p.Glu669Gln
ENST00000373322.1:c.2005G>C	ENSP00000362419.1:p.Glu669Gln
ENST00000373324.8:c.1924G>C	ENSP00000362421.4:p.Glu642Gln
ENST00000483302.5:n.1227G>C
NM_001005373.3:c.2005G>C	NP_001005373.1:p.Glu669Gln
NM_001005374.3:c.2005G>C	NP_001005374.1:p.Glu669Gln
NM_001190723.2:c.1924G>C	NP_001177652.1:p.Glu642Gln
NM_138361.5:c.2005G>C , LRG_373t1:c.2005G>C	NP_612370.3:p.Glu669Gln
XM_006717316.2:c.1906G>C	XP_006717379.1:p.Glu636Gln
XM_006717316.4:c.1906G>C	XP_006717379.1:p.Glu636Gln
XM_017015283.1:c.2005G>C	XP_016870772.1:p.Glu669Gln
XM_017015284.2:c.1216G>C	XP_016870773.1:p.Glu406Gln
XR_001746415.2:n.2540G>C
XR_929874.3:n.2364G>C
NM_001190723.3:c.1924G>C	NP_001177652.1:p.Glu642Gln
NM_001005373.4:c.2005G>C MANE Select	NP_001005373.1:p.Glu669Gln
NM_001005374.4:c.2005G>C	NP_001005374.1:p.Glu669Gln
NM_001384142.1:c.2005G>C	NP_001371071.1:p.Glu669Gln
NM_001384143.1:c.1906G>C	NP_001371072.1:p.Glu636Gln
NM_001384144.1:c.1216G>C	NP_001371073.1:p.Glu406Gln
NR_168891.1:n.2534G>C
NR_168892.1:n.2358G>C