Canonical Allele Identifier: CA374938200

Gene: LRSAM1

Linked Data

• dbSNP Id: rs1345023863
• gnomAD v2: 9-130263334-A-G
• gnomAD v4: 9-127501055-A-G
• MyVariant Identifiers: chr9:g.130263334A>G (hg19) ; chr9:g.127501055A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501055A>G , CM000671.2:g.127501055A>G	GRCh38
NC_000009.11:g.130263334A>G , CM000671.1:g.130263334A>G	GRCh37
NC_000009.10:g.129303155A>G	NCBI36
NG_032008.1:g.54570A>G , LRG_373:g.54570A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1958A>G MANE Select	ENSP00000300417.6:p.Gln653Arg
ENST00000472068.2:c.*1682A>G	ENSP00000501555.1:n.*1682A>G
ENST00000483302.6:n.2623A>G
ENST00000498513.6:c.*849A>G	ENSP00000501637.1:n.*849A>G
ENST00000674511.1:n.1557A>G
ENST00000674516.1:c.*574A>G	ENSP00000502441.1:n.*574A>G
ENST00000674621.1:n.1861-2318A>G
ENST00000674771.1:c.*601A>G	ENSP00000502627.1:n.*601A>G
ENST00000674784.1:c.*1018A>G	ENSP00000501837.1:n.*1018A>G
ENST00000674970.1:c.*1732A>G	ENSP00000502493.1:n.*1732A>G
ENST00000675012.1:n.1902A>G
ENST00000675141.1:c.1859A>G	ENSP00000502420.1:p.Gln620Arg
ENST00000675198.1:n.1838A>G
ENST00000675213.1:c.1913A>G	ENSP00000502218.1:p.Gln638Arg
ENST00000675224.1:c.*24A>G	ENSP00000501869.1:n.*24A>G
ENST00000675253.1:c.*630A>G	ENSP00000502557.1:n.*630A>G
ENST00000675445.1:c.*1630A>G	ENSP00000502253.1:n.*1630A>G
ENST00000675448.1:c.1958A>G	ENSP00000502167.1:p.Gln653Arg
ENST00000675521.1:n.1868A>G
ENST00000675572.1:c.1859A>G	ENSP00000501598.1:p.Gln620Arg
ENST00000675641.1:c.*700A>G	ENSP00000501845.1:n.*700A>G
ENST00000675657.1:c.*571A>G	ENSP00000502002.1:n.*571A>G
ENST00000675662.1:n.1753A>G
ENST00000675789.1:c.1778A>G	ENSP00000501954.1:p.Gln593Arg
ENST00000675883.1:c.1877A>G	ENSP00000501592.1:p.Gln626Arg
ENST00000675945.1:c.*599A>G	ENSP00000501835.1:n.*599A>G
ENST00000676014.1:c.1901A>G	ENSP00000502058.1:p.Gln634Arg
ENST00000676035.1:n.1620A>G
ENST00000676106.1:n.1995A>G
ENST00000676137.1:n.1988A>G
ENST00000676170.1:c.2039A>G	ENSP00000502177.1:p.Gln680Arg
ENST00000676318.1:c.*2788A>G	ENSP00000502300.1:n.*2788A>G
ENST00000676336.1:c.*571A>G	ENSP00000502686.1:n.*571A>G
ENST00000676349.1:c.*1646A>G	ENSP00000502155.1:n.*1646A>G
ENST00000676399.1:n.1861A>G
ENST00000676409.1:n.2018A>G
ENST00000300417.10:c.1958A>G	ENSP00000300417.6:p.Gln653Arg
ENST00000323301.8:c.1958A>G	ENSP00000322937.4:p.Gln653Arg
ENST00000373322.1:c.1958A>G	ENSP00000362419.1:p.Gln653Arg
ENST00000373324.8:c.1877A>G	ENSP00000362421.4:p.Gln626Arg
ENST00000483302.5:n.1180A>G
NM_001005373.3:c.1958A>G	NP_001005373.1:p.Gln653Arg
NM_001005374.3:c.1958A>G	NP_001005374.1:p.Gln653Arg
NM_001190723.2:c.1877A>G	NP_001177652.1:p.Gln626Arg
NM_138361.5:c.1958A>G , LRG_373t1:c.1958A>G	NP_612370.3:p.Gln653Arg
XM_006717316.2:c.1859A>G	XP_006717379.1:p.Gln620Arg
XM_006717316.4:c.1859A>G	XP_006717379.1:p.Gln620Arg
XM_017015283.1:c.1958A>G	XP_016870772.1:p.Gln653Arg
XM_017015284.2:c.1169A>G	XP_016870773.1:p.Gln390Arg
XR_001746415.2:n.2493A>G
XR_929874.3:n.2317A>G
NM_001190723.3:c.1877A>G	NP_001177652.1:p.Gln626Arg
NM_001005373.4:c.1958A>G MANE Select	NP_001005373.1:p.Gln653Arg
NM_001005374.4:c.1958A>G	NP_001005374.1:p.Gln653Arg
NM_001384142.1:c.1958A>G	NP_001371071.1:p.Gln653Arg
NM_001384143.1:c.1859A>G	NP_001371072.1:p.Gln620Arg
NM_001384144.1:c.1169A>G	NP_001371073.1:p.Gln390Arg
NR_168891.1:n.2487A>G
NR_168892.1:n.2311A>G