Canonical Allele Identifier: CA374938282

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263376A>T (hg19) ; chr9:g.127501097A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501097A>T , CM000671.2:g.127501097A>T	GRCh38
NC_000009.11:g.130263376A>T , CM000671.1:g.130263376A>T	GRCh37
NC_000009.10:g.129303197A>T	NCBI36
NG_032008.1:g.54612A>T , LRG_373:g.54612A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2000A>T MANE Select	ENSP00000300417.6:p.Glu667Val
ENST00000472068.2:c.*1724A>T	ENSP00000501555.1:n.*1724A>T
ENST00000483302.6:n.2665A>T
ENST00000498513.6:c.*891A>T	ENSP00000501637.1:n.*891A>T
ENST00000674511.1:n.1599A>T
ENST00000674516.1:c.*616A>T	ENSP00000502441.1:n.*616A>T
ENST00000674621.1:n.1861-2276A>T
ENST00000674771.1:c.*643A>T	ENSP00000502627.1:n.*643A>T
ENST00000674784.1:c.*1060A>T	ENSP00000501837.1:n.*1060A>T
ENST00000674970.1:c.*1774A>T	ENSP00000502493.1:n.*1774A>T
ENST00000675012.1:n.1944A>T
ENST00000675141.1:c.1901A>T	ENSP00000502420.1:p.Glu634Val
ENST00000675198.1:n.1880A>T
ENST00000675213.1:c.1955A>T	ENSP00000502218.1:p.Glu652Val
ENST00000675224.1:c.*66A>T	ENSP00000501869.1:n.*66A>T
ENST00000675253.1:c.*672A>T	ENSP00000502557.1:n.*672A>T
ENST00000675445.1:c.*1672A>T	ENSP00000502253.1:n.*1672A>T
ENST00000675448.1:c.2000A>T	ENSP00000502167.1:p.Glu667Val
ENST00000675521.1:n.1910A>T
ENST00000675572.1:c.1901A>T	ENSP00000501598.1:p.Glu634Val
ENST00000675641.1:c.*742A>T	ENSP00000501845.1:n.*742A>T
ENST00000675657.1:c.*613A>T	ENSP00000502002.1:n.*613A>T
ENST00000675662.1:n.1795A>T
ENST00000675789.1:c.1820A>T	ENSP00000501954.1:p.Glu607Val
ENST00000675883.1:c.1919A>T	ENSP00000501592.1:p.Glu640Val
ENST00000675945.1:c.*641A>T	ENSP00000501835.1:n.*641A>T
ENST00000676014.1:c.1943A>T	ENSP00000502058.1:p.Glu648Val
ENST00000676035.1:n.1662A>T
ENST00000676106.1:n.2037A>T
ENST00000676137.1:n.2030A>T
ENST00000676170.1:c.2081A>T	ENSP00000502177.1:p.Glu694Val
ENST00000676318.1:c.*2830A>T	ENSP00000502300.1:n.*2830A>T
ENST00000676336.1:c.*613A>T	ENSP00000502686.1:n.*613A>T
ENST00000676349.1:c.*1688A>T	ENSP00000502155.1:n.*1688A>T
ENST00000676399.1:n.1903A>T
ENST00000676409.1:n.2060A>T
ENST00000300417.10:c.2000A>T	ENSP00000300417.6:p.Glu667Val
ENST00000323301.8:c.2000A>T	ENSP00000322937.4:p.Glu667Val
ENST00000373322.1:c.2000A>T	ENSP00000362419.1:p.Glu667Val
ENST00000373324.8:c.1919A>T	ENSP00000362421.4:p.Glu640Val
ENST00000483302.5:n.1222A>T
NM_001005373.3:c.2000A>T	NP_001005373.1:p.Glu667Val
NM_001005374.3:c.2000A>T	NP_001005374.1:p.Glu667Val
NM_001190723.2:c.1919A>T	NP_001177652.1:p.Glu640Val
NM_138361.5:c.2000A>T , LRG_373t1:c.2000A>T	NP_612370.3:p.Glu667Val
XM_006717316.2:c.1901A>T	XP_006717379.1:p.Glu634Val
XM_006717316.4:c.1901A>T	XP_006717379.1:p.Glu634Val
XM_017015283.1:c.2000A>T	XP_016870772.1:p.Glu667Val
XM_017015284.2:c.1211A>T	XP_016870773.1:p.Glu404Val
XR_001746415.2:n.2535A>T
XR_929874.3:n.2359A>T
NM_001190723.3:c.1919A>T	NP_001177652.1:p.Glu640Val
NM_001005373.4:c.2000A>T MANE Select	NP_001005373.1:p.Glu667Val
NM_001005374.4:c.2000A>T	NP_001005374.1:p.Glu667Val
NM_001384142.1:c.2000A>T	NP_001371071.1:p.Glu667Val
NM_001384143.1:c.1901A>T	NP_001371072.1:p.Glu634Val
NM_001384144.1:c.1211A>T	NP_001371073.1:p.Glu404Val
NR_168891.1:n.2529A>T
NR_168892.1:n.2353A>T