Canonical Allele Identifier: CA467236775

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263354A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501075A>C , CM000671.2:g.127501075A>C	GRCh38
NC_000009.11:g.130263354A>C , CM000671.1:g.130263354A>C	GRCh37
NC_000009.10:g.129303175A>C	NCBI36
NG_032008.1:g.54590A>C , LRG_373:g.54590A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1978A>C MANE Select	ENSP00000300417.6:p.Arg660=
ENST00000472068.2:c.*1702A>C	ENSP00000501555.1:n.*1702A>C
ENST00000483302.6:n.2643A>C
ENST00000498513.6:c.*869A>C	ENSP00000501637.1:n.*869A>C
ENST00000674511.1:n.1577A>C
ENST00000674516.1:c.*594A>C	ENSP00000502441.1:n.*594A>C
ENST00000674621.1:n.1861-2298A>C
ENST00000674771.1:c.*621A>C	ENSP00000502627.1:n.*621A>C
ENST00000674784.1:c.*1038A>C	ENSP00000501837.1:n.*1038A>C
ENST00000674970.1:c.*1752A>C	ENSP00000502493.1:n.*1752A>C
ENST00000675012.1:n.1922A>C
ENST00000675141.1:c.1879A>C	ENSP00000502420.1:p.Arg627=
ENST00000675198.1:n.1858A>C
ENST00000675213.1:c.1933A>C	ENSP00000502218.1:p.Arg645=
ENST00000675224.1:c.*44A>C	ENSP00000501869.1:n.*44A>C
ENST00000675253.1:c.*650A>C	ENSP00000502557.1:n.*650A>C
ENST00000675445.1:c.*1650A>C	ENSP00000502253.1:n.*1650A>C
ENST00000675448.1:c.1978A>C	ENSP00000502167.1:p.Arg660=
ENST00000675521.1:n.1888A>C
ENST00000675572.1:c.1879A>C	ENSP00000501598.1:p.Arg627=
ENST00000675641.1:c.*720A>C	ENSP00000501845.1:n.*720A>C
ENST00000675657.1:c.*591A>C	ENSP00000502002.1:n.*591A>C
ENST00000675662.1:n.1773A>C
ENST00000675789.1:c.1798A>C	ENSP00000501954.1:p.Arg600=
ENST00000675883.1:c.1897A>C	ENSP00000501592.1:p.Arg633=
ENST00000675945.1:c.*619A>C	ENSP00000501835.1:n.*619A>C
ENST00000676014.1:c.1921A>C	ENSP00000502058.1:p.Arg641=
ENST00000676035.1:n.1640A>C
ENST00000676106.1:n.2015A>C
ENST00000676137.1:n.2008A>C
ENST00000676170.1:c.2059A>C	ENSP00000502177.1:p.Arg687=
ENST00000676318.1:c.*2808A>C	ENSP00000502300.1:n.*2808A>C
ENST00000676336.1:c.*591A>C	ENSP00000502686.1:n.*591A>C
ENST00000676349.1:c.*1666A>C	ENSP00000502155.1:n.*1666A>C
ENST00000676399.1:n.1881A>C
ENST00000676409.1:n.2038A>C
ENST00000300417.10:c.1978A>C	ENSP00000300417.6:p.Arg660=
ENST00000323301.8:c.1978A>C	ENSP00000322937.4:p.Arg660=
ENST00000373322.1:c.1978A>C	ENSP00000362419.1:p.Arg660=
ENST00000373324.8:c.1897A>C	ENSP00000362421.4:p.Arg633=
ENST00000483302.5:n.1200A>C
NM_001005373.3:c.1978A>C	NP_001005373.1:p.Arg660=
NM_001005374.3:c.1978A>C	NP_001005374.1:p.Arg660=
NM_001190723.2:c.1897A>C	NP_001177652.1:p.Arg633=
NM_138361.5:c.1978A>C , LRG_373t1:c.1978A>C	NP_612370.3:p.Arg660=
XM_006717316.2:c.1879A>C	XP_006717379.1:p.Arg627=
XM_006717316.4:c.1879A>C	XP_006717379.1:p.Arg627=
XM_017015283.1:c.1978A>C	XP_016870772.1:p.Arg660=
XM_017015284.2:c.1189A>C	XP_016870773.1:p.Arg397=
XR_001746415.2:n.2513A>C
XR_929874.3:n.2337A>C
NM_001190723.3:c.1897A>C	NP_001177652.1:p.Arg633=
NM_001005373.4:c.1978A>C MANE Select	NP_001005373.1:p.Arg660=
NM_001005374.4:c.1978A>C	NP_001005374.1:p.Arg660=
NM_001384142.1:c.1978A>C	NP_001371071.1:p.Arg660=
NM_001384143.1:c.1879A>C	NP_001371072.1:p.Arg627=
NM_001384144.1:c.1189A>C	NP_001371073.1:p.Arg397=
NR_168891.1:n.2507A>C
NR_168892.1:n.2331A>C