Canonical Allele Identifier: CA374938245

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263355G>C (hg19) ; chr9:g.127501076G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501076G>C , CM000671.2:g.127501076G>C	GRCh38
NC_000009.11:g.130263355G>C , CM000671.1:g.130263355G>C	GRCh37
NC_000009.10:g.129303176G>C	NCBI36
NG_032008.1:g.54591G>C , LRG_373:g.54591G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1979G>C MANE Select	ENSP00000300417.6:p.Arg660Thr
ENST00000472068.2:c.*1703G>C	ENSP00000501555.1:n.*1703G>C
ENST00000483302.6:n.2644G>C
ENST00000498513.6:c.*870G>C	ENSP00000501637.1:n.*870G>C
ENST00000674511.1:n.1578G>C
ENST00000674516.1:c.*595G>C	ENSP00000502441.1:n.*595G>C
ENST00000674621.1:n.1861-2297G>C
ENST00000674771.1:c.*622G>C	ENSP00000502627.1:n.*622G>C
ENST00000674784.1:c.*1039G>C	ENSP00000501837.1:n.*1039G>C
ENST00000674970.1:c.*1753G>C	ENSP00000502493.1:n.*1753G>C
ENST00000675012.1:n.1923G>C
ENST00000675141.1:c.1880G>C	ENSP00000502420.1:p.Arg627Thr
ENST00000675198.1:n.1859G>C
ENST00000675213.1:c.1934G>C	ENSP00000502218.1:p.Arg645Thr
ENST00000675224.1:c.*45G>C	ENSP00000501869.1:n.*45G>C
ENST00000675253.1:c.*651G>C	ENSP00000502557.1:n.*651G>C
ENST00000675445.1:c.*1651G>C	ENSP00000502253.1:n.*1651G>C
ENST00000675448.1:c.1979G>C	ENSP00000502167.1:p.Arg660Thr
ENST00000675521.1:n.1889G>C
ENST00000675572.1:c.1880G>C	ENSP00000501598.1:p.Arg627Thr
ENST00000675641.1:c.*721G>C	ENSP00000501845.1:n.*721G>C
ENST00000675657.1:c.*592G>C	ENSP00000502002.1:n.*592G>C
ENST00000675662.1:n.1774G>C
ENST00000675789.1:c.1799G>C	ENSP00000501954.1:p.Arg600Thr
ENST00000675883.1:c.1898G>C	ENSP00000501592.1:p.Arg633Thr
ENST00000675945.1:c.*620G>C	ENSP00000501835.1:n.*620G>C
ENST00000676014.1:c.1922G>C	ENSP00000502058.1:p.Arg641Thr
ENST00000676035.1:n.1641G>C
ENST00000676106.1:n.2016G>C
ENST00000676137.1:n.2009G>C
ENST00000676170.1:c.2060G>C	ENSP00000502177.1:p.Arg687Thr
ENST00000676318.1:c.*2809G>C	ENSP00000502300.1:n.*2809G>C
ENST00000676336.1:c.*592G>C	ENSP00000502686.1:n.*592G>C
ENST00000676349.1:c.*1667G>C	ENSP00000502155.1:n.*1667G>C
ENST00000676399.1:n.1882G>C
ENST00000676409.1:n.2039G>C
ENST00000300417.10:c.1979G>C	ENSP00000300417.6:p.Arg660Thr
ENST00000323301.8:c.1979G>C	ENSP00000322937.4:p.Arg660Thr
ENST00000373322.1:c.1979G>C	ENSP00000362419.1:p.Arg660Thr
ENST00000373324.8:c.1898G>C	ENSP00000362421.4:p.Arg633Thr
ENST00000483302.5:n.1201G>C
NM_001005373.3:c.1979G>C	NP_001005373.1:p.Arg660Thr
NM_001005374.3:c.1979G>C	NP_001005374.1:p.Arg660Thr
NM_001190723.2:c.1898G>C	NP_001177652.1:p.Arg633Thr
NM_138361.5:c.1979G>C , LRG_373t1:c.1979G>C	NP_612370.3:p.Arg660Thr
XM_006717316.2:c.1880G>C	XP_006717379.1:p.Arg627Thr
XM_006717316.4:c.1880G>C	XP_006717379.1:p.Arg627Thr
XM_017015283.1:c.1979G>C	XP_016870772.1:p.Arg660Thr
XM_017015284.2:c.1190G>C	XP_016870773.1:p.Arg397Thr
XR_001746415.2:n.2514G>C
XR_929874.3:n.2338G>C
NM_001190723.3:c.1898G>C	NP_001177652.1:p.Arg633Thr
NM_001005373.4:c.1979G>C MANE Select	NP_001005373.1:p.Arg660Thr
NM_001005374.4:c.1979G>C	NP_001005374.1:p.Arg660Thr
NM_001384142.1:c.1979G>C	NP_001371071.1:p.Arg660Thr
NM_001384143.1:c.1880G>C	NP_001371072.1:p.Arg627Thr
NM_001384144.1:c.1190G>C	NP_001371073.1:p.Arg397Thr
NR_168891.1:n.2508G>C
NR_168892.1:n.2332G>C