Canonical Allele Identifier: CA374938208

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263337A>C (hg19) ; chr9:g.127501058A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501058A>C , CM000671.2:g.127501058A>C	GRCh38
NC_000009.11:g.130263337A>C , CM000671.1:g.130263337A>C	GRCh37
NC_000009.10:g.129303158A>C	NCBI36
NG_032008.1:g.54573A>C , LRG_373:g.54573A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1961A>C MANE Select	ENSP00000300417.6:p.Glu654Ala
ENST00000472068.2:c.*1685A>C	ENSP00000501555.1:n.*1685A>C
ENST00000483302.6:n.2626A>C
ENST00000498513.6:c.*852A>C	ENSP00000501637.1:n.*852A>C
ENST00000674511.1:n.1560A>C
ENST00000674516.1:c.*577A>C	ENSP00000502441.1:n.*577A>C
ENST00000674621.1:n.1861-2315A>C
ENST00000674771.1:c.*604A>C	ENSP00000502627.1:n.*604A>C
ENST00000674784.1:c.*1021A>C	ENSP00000501837.1:n.*1021A>C
ENST00000674970.1:c.*1735A>C	ENSP00000502493.1:n.*1735A>C
ENST00000675012.1:n.1905A>C
ENST00000675141.1:c.1862A>C	ENSP00000502420.1:p.Glu621Ala
ENST00000675198.1:n.1841A>C
ENST00000675213.1:c.1916A>C	ENSP00000502218.1:p.Glu639Ala
ENST00000675224.1:c.*27A>C	ENSP00000501869.1:n.*27A>C
ENST00000675253.1:c.*633A>C	ENSP00000502557.1:n.*633A>C
ENST00000675445.1:c.*1633A>C	ENSP00000502253.1:n.*1633A>C
ENST00000675448.1:c.1961A>C	ENSP00000502167.1:p.Glu654Ala
ENST00000675521.1:n.1871A>C
ENST00000675572.1:c.1862A>C	ENSP00000501598.1:p.Glu621Ala
ENST00000675641.1:c.*703A>C	ENSP00000501845.1:n.*703A>C
ENST00000675657.1:c.*574A>C	ENSP00000502002.1:n.*574A>C
ENST00000675662.1:n.1756A>C
ENST00000675789.1:c.1781A>C	ENSP00000501954.1:p.Glu594Ala
ENST00000675883.1:c.1880A>C	ENSP00000501592.1:p.Glu627Ala
ENST00000675945.1:c.*602A>C	ENSP00000501835.1:n.*602A>C
ENST00000676014.1:c.1904A>C	ENSP00000502058.1:p.Glu635Ala
ENST00000676035.1:n.1623A>C
ENST00000676106.1:n.1998A>C
ENST00000676137.1:n.1991A>C
ENST00000676170.1:c.2042A>C	ENSP00000502177.1:p.Glu681Ala
ENST00000676318.1:c.*2791A>C	ENSP00000502300.1:n.*2791A>C
ENST00000676336.1:c.*574A>C	ENSP00000502686.1:n.*574A>C
ENST00000676349.1:c.*1649A>C	ENSP00000502155.1:n.*1649A>C
ENST00000676399.1:n.1864A>C
ENST00000676409.1:n.2021A>C
ENST00000300417.10:c.1961A>C	ENSP00000300417.6:p.Glu654Ala
ENST00000323301.8:c.1961A>C	ENSP00000322937.4:p.Glu654Ala
ENST00000373322.1:c.1961A>C	ENSP00000362419.1:p.Glu654Ala
ENST00000373324.8:c.1880A>C	ENSP00000362421.4:p.Glu627Ala
ENST00000483302.5:n.1183A>C
NM_001005373.3:c.1961A>C	NP_001005373.1:p.Glu654Ala
NM_001005374.3:c.1961A>C	NP_001005374.1:p.Glu654Ala
NM_001190723.2:c.1880A>C	NP_001177652.1:p.Glu627Ala
NM_138361.5:c.1961A>C , LRG_373t1:c.1961A>C	NP_612370.3:p.Glu654Ala
XM_006717316.2:c.1862A>C	XP_006717379.1:p.Glu621Ala
XM_006717316.4:c.1862A>C	XP_006717379.1:p.Glu621Ala
XM_017015283.1:c.1961A>C	XP_016870772.1:p.Glu654Ala
XM_017015284.2:c.1172A>C	XP_016870773.1:p.Glu391Ala
XR_001746415.2:n.2496A>C
XR_929874.3:n.2320A>C
NM_001190723.3:c.1880A>C	NP_001177652.1:p.Glu627Ala
NM_001005373.4:c.1961A>C MANE Select	NP_001005373.1:p.Glu654Ala
NM_001005374.4:c.1961A>C	NP_001005374.1:p.Glu654Ala
NM_001384142.1:c.1961A>C	NP_001371071.1:p.Glu654Ala
NM_001384143.1:c.1862A>C	NP_001371072.1:p.Glu621Ala
NM_001384144.1:c.1172A>C	NP_001371073.1:p.Glu391Ala
NR_168891.1:n.2490A>C
NR_168892.1:n.2314A>C