Canonical Allele Identifier: CA467236881

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263380G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501101G>C , CM000671.2:g.127501101G>C	GRCh38
NC_000009.11:g.130263380G>C , CM000671.1:g.130263380G>C	GRCh37
NC_000009.10:g.129303201G>C	NCBI36
NG_032008.1:g.54616G>C , LRG_373:g.54616G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2004G>C MANE Select	ENSP00000300417.6:p.Leu668=
ENST00000472068.2:c.*1728G>C	ENSP00000501555.1:n.*1728G>C
ENST00000483302.6:n.2669G>C
ENST00000498513.6:c.*895G>C	ENSP00000501637.1:n.*895G>C
ENST00000674511.1:n.1603G>C
ENST00000674516.1:c.*620G>C	ENSP00000502441.1:n.*620G>C
ENST00000674621.1:n.1861-2272G>C
ENST00000674771.1:c.*647G>C	ENSP00000502627.1:n.*647G>C
ENST00000674784.1:c.*1064G>C	ENSP00000501837.1:n.*1064G>C
ENST00000674970.1:c.*1778G>C	ENSP00000502493.1:n.*1778G>C
ENST00000675012.1:n.1948G>C
ENST00000675141.1:c.1905G>C	ENSP00000502420.1:p.Leu635=
ENST00000675198.1:n.1884G>C
ENST00000675213.1:c.1959G>C	ENSP00000502218.1:p.Leu653=
ENST00000675224.1:c.*70G>C	ENSP00000501869.1:n.*70G>C
ENST00000675253.1:c.*676G>C	ENSP00000502557.1:n.*676G>C
ENST00000675445.1:c.*1676G>C	ENSP00000502253.1:n.*1676G>C
ENST00000675448.1:c.2004G>C	ENSP00000502167.1:p.Leu668=
ENST00000675521.1:n.1914G>C
ENST00000675572.1:c.1905G>C	ENSP00000501598.1:p.Leu635=
ENST00000675641.1:c.*746G>C	ENSP00000501845.1:n.*746G>C
ENST00000675657.1:c.*617G>C	ENSP00000502002.1:n.*617G>C
ENST00000675662.1:n.1799G>C
ENST00000675789.1:c.1824G>C	ENSP00000501954.1:p.Leu608=
ENST00000675883.1:c.1923G>C	ENSP00000501592.1:p.Leu641=
ENST00000675945.1:c.*645G>C	ENSP00000501835.1:n.*645G>C
ENST00000676014.1:c.1947G>C	ENSP00000502058.1:p.Leu649=
ENST00000676035.1:n.1666G>C
ENST00000676106.1:n.2041G>C
ENST00000676137.1:n.2034G>C
ENST00000676170.1:c.2085G>C	ENSP00000502177.1:p.Leu695=
ENST00000676318.1:c.*2834G>C	ENSP00000502300.1:n.*2834G>C
ENST00000676336.1:c.*617G>C	ENSP00000502686.1:n.*617G>C
ENST00000676349.1:c.*1692G>C	ENSP00000502155.1:n.*1692G>C
ENST00000676399.1:n.1907G>C
ENST00000676409.1:n.2064G>C
ENST00000300417.10:c.2004G>C	ENSP00000300417.6:p.Leu668=
ENST00000323301.8:c.2004G>C	ENSP00000322937.4:p.Leu668=
ENST00000373322.1:c.2004G>C	ENSP00000362419.1:p.Leu668=
ENST00000373324.8:c.1923G>C	ENSP00000362421.4:p.Leu641=
ENST00000483302.5:n.1226G>C
NM_001005373.3:c.2004G>C	NP_001005373.1:p.Leu668=
NM_001005374.3:c.2004G>C	NP_001005374.1:p.Leu668=
NM_001190723.2:c.1923G>C	NP_001177652.1:p.Leu641=
NM_138361.5:c.2004G>C , LRG_373t1:c.2004G>C	NP_612370.3:p.Leu668=
XM_006717316.2:c.1905G>C	XP_006717379.1:p.Leu635=
XM_006717316.4:c.1905G>C	XP_006717379.1:p.Leu635=
XM_017015283.1:c.2004G>C	XP_016870772.1:p.Leu668=
XM_017015284.2:c.1215G>C	XP_016870773.1:p.Leu405=
XR_001746415.2:n.2539G>C
XR_929874.3:n.2363G>C
NM_001190723.3:c.1923G>C	NP_001177652.1:p.Leu641=
NM_001005373.4:c.2004G>C MANE Select	NP_001005373.1:p.Leu668=
NM_001005374.4:c.2004G>C	NP_001005374.1:p.Leu668=
NM_001384142.1:c.2004G>C	NP_001371071.1:p.Leu668=
NM_001384143.1:c.1905G>C	NP_001371072.1:p.Leu635=
NM_001384144.1:c.1215G>C	NP_001371073.1:p.Leu405=
NR_168891.1:n.2533G>C
NR_168892.1:n.2357G>C