Canonical Allele Identifier: CA374938116

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263289A>G (hg19) ; chr9:g.127501010A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501010A>G , CM000671.2:g.127501010A>G	GRCh38
NC_000009.11:g.130263289A>G , CM000671.1:g.130263289A>G	GRCh37
NC_000009.10:g.129303110A>G	NCBI36
NG_032008.1:g.54525A>G , LRG_373:g.54525A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1913A>G MANE Select	ENSP00000300417.6:p.Glu638Gly
ENST00000472068.2:c.*1637A>G	ENSP00000501555.1:n.*1637A>G
ENST00000483302.6:n.2578A>G
ENST00000498513.6:c.*804A>G	ENSP00000501637.1:n.*804A>G
ENST00000674511.1:n.1512A>G
ENST00000674516.1:c.*529A>G	ENSP00000502441.1:n.*529A>G
ENST00000674621.1:n.1861-2363A>G
ENST00000674771.1:c.*556A>G	ENSP00000502627.1:n.*556A>G
ENST00000674784.1:c.*973A>G	ENSP00000501837.1:n.*973A>G
ENST00000674970.1:c.*1687A>G	ENSP00000502493.1:n.*1687A>G
ENST00000675012.1:n.1857A>G
ENST00000675141.1:c.1814A>G	ENSP00000502420.1:p.Glu605Gly
ENST00000675198.1:n.1793A>G
ENST00000675213.1:c.1868A>G	ENSP00000502218.1:p.Glu623Gly
ENST00000675224.1:c.1941A>G	ENSP00000501869.1:p.Arg647=
ENST00000675253.1:c.*585A>G	ENSP00000502557.1:n.*585A>G
ENST00000675445.1:c.*1585A>G	ENSP00000502253.1:n.*1585A>G
ENST00000675448.1:c.1913A>G	ENSP00000502167.1:p.Glu638Gly
ENST00000675521.1:n.1823A>G
ENST00000675572.1:c.1814A>G	ENSP00000501598.1:p.Glu605Gly
ENST00000675641.1:c.*655A>G	ENSP00000501845.1:n.*655A>G
ENST00000675657.1:c.*526A>G	ENSP00000502002.1:n.*526A>G
ENST00000675662.1:n.1708A>G
ENST00000675789.1:c.1733A>G	ENSP00000501954.1:p.Glu578Gly
ENST00000675883.1:c.1832A>G	ENSP00000501592.1:p.Glu611Gly
ENST00000675945.1:c.*554A>G	ENSP00000501835.1:n.*554A>G
ENST00000676014.1:c.1856A>G	ENSP00000502058.1:p.Glu619Gly
ENST00000676035.1:n.1575A>G
ENST00000676106.1:n.1950A>G
ENST00000676137.1:n.1943A>G
ENST00000676170.1:c.1994A>G	ENSP00000502177.1:p.Glu665Gly
ENST00000676318.1:c.*2743A>G	ENSP00000502300.1:n.*2743A>G
ENST00000676336.1:c.*526A>G	ENSP00000502686.1:n.*526A>G
ENST00000676349.1:c.*1601A>G	ENSP00000502155.1:n.*1601A>G
ENST00000676399.1:n.1816A>G
ENST00000676409.1:n.1973A>G
ENST00000300417.10:c.1913A>G	ENSP00000300417.6:p.Glu638Gly
ENST00000323301.8:c.1913A>G	ENSP00000322937.4:p.Glu638Gly
ENST00000373322.1:c.1913A>G	ENSP00000362419.1:p.Glu638Gly
ENST00000373324.8:c.1832A>G	ENSP00000362421.4:p.Glu611Gly
ENST00000472068.1:n.806A>G
ENST00000483302.5:n.1135A>G
NM_001005373.3:c.1913A>G	NP_001005373.1:p.Glu638Gly
NM_001005374.3:c.1913A>G	NP_001005374.1:p.Glu638Gly
NM_001190723.2:c.1832A>G	NP_001177652.1:p.Glu611Gly
NM_138361.5:c.1913A>G , LRG_373t1:c.1913A>G	NP_612370.3:p.Glu638Gly
XM_006717316.2:c.1814A>G	XP_006717379.1:p.Glu605Gly
XM_006717316.4:c.1814A>G	XP_006717379.1:p.Glu605Gly
XM_017015283.1:c.1913A>G	XP_016870772.1:p.Glu638Gly
XM_017015284.2:c.1124A>G	XP_016870773.1:p.Glu375Gly
XR_001746415.2:n.2448A>G
XR_929874.3:n.2272A>G
NM_001190723.3:c.1832A>G	NP_001177652.1:p.Glu611Gly
NM_001005373.4:c.1913A>G MANE Select	NP_001005373.1:p.Glu638Gly
NM_001005374.4:c.1913A>G	NP_001005374.1:p.Glu638Gly
NM_001384142.1:c.1913A>G	NP_001371071.1:p.Glu638Gly
NM_001384143.1:c.1814A>G	NP_001371072.1:p.Glu605Gly
NM_001384144.1:c.1124A>G	NP_001371073.1:p.Glu375Gly
NR_168891.1:n.2442A>G
NR_168892.1:n.2266A>G