Canonical Allele Identifier: CA199852964

Gene: LRSAM1

Linked Data

• dbSNP Id: rs1042197619
• MyVariant Identifiers: chr9:g.130263370C>G (hg19) ; chr9:g.127501091C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501091C>G , CM000671.2:g.127501091C>G	GRCh38
NC_000009.11:g.130263370C>G , CM000671.1:g.130263370C>G	GRCh37
NC_000009.10:g.129303191C>G	NCBI36
NG_032008.1:g.54606C>G , LRG_373:g.54606C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1994C>G MANE Select	ENSP00000300417.6:p.Pro665Arg
ENST00000472068.2:c.*1718C>G	ENSP00000501555.1:n.*1718C>G
ENST00000483302.6:n.2659C>G
ENST00000498513.6:c.*885C>G	ENSP00000501637.1:n.*885C>G
ENST00000674511.1:n.1593C>G
ENST00000674516.1:c.*610C>G	ENSP00000502441.1:n.*610C>G
ENST00000674621.1:n.1861-2282C>G
ENST00000674771.1:c.*637C>G	ENSP00000502627.1:n.*637C>G
ENST00000674784.1:c.*1054C>G	ENSP00000501837.1:n.*1054C>G
ENST00000674970.1:c.*1768C>G	ENSP00000502493.1:n.*1768C>G
ENST00000675012.1:n.1938C>G
ENST00000675141.1:c.1895C>G	ENSP00000502420.1:p.Pro632Arg
ENST00000675198.1:n.1874C>G
ENST00000675213.1:c.1949C>G	ENSP00000502218.1:p.Pro650Arg
ENST00000675224.1:c.*60C>G	ENSP00000501869.1:n.*60C>G
ENST00000675253.1:c.*666C>G	ENSP00000502557.1:n.*666C>G
ENST00000675445.1:c.*1666C>G	ENSP00000502253.1:n.*1666C>G
ENST00000675448.1:c.1994C>G	ENSP00000502167.1:p.Pro665Arg
ENST00000675521.1:n.1904C>G
ENST00000675572.1:c.1895C>G	ENSP00000501598.1:p.Pro632Arg
ENST00000675641.1:c.*736C>G	ENSP00000501845.1:n.*736C>G
ENST00000675657.1:c.*607C>G	ENSP00000502002.1:n.*607C>G
ENST00000675662.1:n.1789C>G
ENST00000675789.1:c.1814C>G	ENSP00000501954.1:p.Pro605Arg
ENST00000675883.1:c.1913C>G	ENSP00000501592.1:p.Pro638Arg
ENST00000675945.1:c.*635C>G	ENSP00000501835.1:n.*635C>G
ENST00000676014.1:c.1937C>G	ENSP00000502058.1:p.Pro646Arg
ENST00000676035.1:n.1656C>G
ENST00000676106.1:n.2031C>G
ENST00000676137.1:n.2024C>G
ENST00000676170.1:c.2075C>G	ENSP00000502177.1:p.Pro692Arg
ENST00000676318.1:c.*2824C>G	ENSP00000502300.1:n.*2824C>G
ENST00000676336.1:c.*607C>G	ENSP00000502686.1:n.*607C>G
ENST00000676349.1:c.*1682C>G	ENSP00000502155.1:n.*1682C>G
ENST00000676399.1:n.1897C>G
ENST00000676409.1:n.2054C>G
ENST00000300417.10:c.1994C>G	ENSP00000300417.6:p.Pro665Arg
ENST00000323301.8:c.1994C>G	ENSP00000322937.4:p.Pro665Arg
ENST00000373322.1:c.1994C>G	ENSP00000362419.1:p.Pro665Arg
ENST00000373324.8:c.1913C>G	ENSP00000362421.4:p.Pro638Arg
ENST00000483302.5:n.1216C>G
NM_001005373.3:c.1994C>G	NP_001005373.1:p.Pro665Arg
NM_001005374.3:c.1994C>G	NP_001005374.1:p.Pro665Arg
NM_001190723.2:c.1913C>G	NP_001177652.1:p.Pro638Arg
NM_138361.5:c.1994C>G , LRG_373t1:c.1994C>G	NP_612370.3:p.Pro665Arg
XM_006717316.2:c.1895C>G	XP_006717379.1:p.Pro632Arg
XM_006717316.4:c.1895C>G	XP_006717379.1:p.Pro632Arg
XM_017015283.1:c.1994C>G	XP_016870772.1:p.Pro665Arg
XM_017015284.2:c.1205C>G	XP_016870773.1:p.Pro402Arg
XR_001746415.2:n.2529C>G
XR_929874.3:n.2353C>G
NM_001190723.3:c.1913C>G	NP_001177652.1:p.Pro638Arg
NM_001005373.4:c.1994C>G MANE Select	NP_001005373.1:p.Pro665Arg
NM_001005374.4:c.1994C>G	NP_001005374.1:p.Pro665Arg
NM_001384142.1:c.1994C>G	NP_001371071.1:p.Pro665Arg
NM_001384143.1:c.1895C>G	NP_001371072.1:p.Pro632Arg
NM_001384144.1:c.1205C>G	NP_001371073.1:p.Pro402Arg
NR_168891.1:n.2523C>G
NR_168892.1:n.2347C>G