Canonical Allele Identifier: CA374938152

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263307G>T (hg19) ; chr9:g.127501028G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501028G>T , CM000671.2:g.127501028G>T	GRCh38
NC_000009.11:g.130263307G>T , CM000671.1:g.130263307G>T	GRCh37
NC_000009.10:g.129303128G>T	NCBI36
NG_032008.1:g.54543G>T , LRG_373:g.54543G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1931G>T MANE Select	ENSP00000300417.6:p.Gly644Val
ENST00000472068.2:c.*1655G>T	ENSP00000501555.1:n.*1655G>T
ENST00000483302.6:n.2596G>T
ENST00000498513.6:c.*822G>T	ENSP00000501637.1:n.*822G>T
ENST00000674511.1:n.1530G>T
ENST00000674516.1:c.*547G>T	ENSP00000502441.1:n.*547G>T
ENST00000674621.1:n.1861-2345G>T
ENST00000674771.1:c.*574G>T	ENSP00000502627.1:n.*574G>T
ENST00000674784.1:c.*991G>T	ENSP00000501837.1:n.*991G>T
ENST00000674970.1:c.*1705G>T	ENSP00000502493.1:n.*1705G>T
ENST00000675012.1:n.1875G>T
ENST00000675141.1:c.1832G>T	ENSP00000502420.1:p.Gly611Val
ENST00000675198.1:n.1811G>T
ENST00000675213.1:c.1886G>T	ENSP00000502218.1:p.Gly629Val
ENST00000675224.1:c.1959G>T	ENSP00000501869.1:p.Gly653=
ENST00000675253.1:c.*603G>T	ENSP00000502557.1:n.*603G>T
ENST00000675445.1:c.*1603G>T	ENSP00000502253.1:n.*1603G>T
ENST00000675448.1:c.1931G>T	ENSP00000502167.1:p.Gly644Val
ENST00000675521.1:n.1841G>T
ENST00000675572.1:c.1832G>T	ENSP00000501598.1:p.Gly611Val
ENST00000675641.1:c.*673G>T	ENSP00000501845.1:n.*673G>T
ENST00000675657.1:c.*544G>T	ENSP00000502002.1:n.*544G>T
ENST00000675662.1:n.1726G>T
ENST00000675789.1:c.1751G>T	ENSP00000501954.1:p.Gly584Val
ENST00000675883.1:c.1850G>T	ENSP00000501592.1:p.Gly617Val
ENST00000675945.1:c.*572G>T	ENSP00000501835.1:n.*572G>T
ENST00000676014.1:c.1874G>T	ENSP00000502058.1:p.Gly625Val
ENST00000676035.1:n.1593G>T
ENST00000676106.1:n.1968G>T
ENST00000676137.1:n.1961G>T
ENST00000676170.1:c.2012G>T	ENSP00000502177.1:p.Gly671Val
ENST00000676318.1:c.*2761G>T	ENSP00000502300.1:n.*2761G>T
ENST00000676336.1:c.*544G>T	ENSP00000502686.1:n.*544G>T
ENST00000676349.1:c.*1619G>T	ENSP00000502155.1:n.*1619G>T
ENST00000676399.1:n.1834G>T
ENST00000676409.1:n.1991G>T
ENST00000300417.10:c.1931G>T	ENSP00000300417.6:p.Gly644Val
ENST00000323301.8:c.1931G>T	ENSP00000322937.4:p.Gly644Val
ENST00000373322.1:c.1931G>T	ENSP00000362419.1:p.Gly644Val
ENST00000373324.8:c.1850G>T	ENSP00000362421.4:p.Gly617Val
ENST00000472068.1:n.824G>T
ENST00000483302.5:n.1153G>T
NM_001005373.3:c.1931G>T	NP_001005373.1:p.Gly644Val
NM_001005374.3:c.1931G>T	NP_001005374.1:p.Gly644Val
NM_001190723.2:c.1850G>T	NP_001177652.1:p.Gly617Val
NM_138361.5:c.1931G>T , LRG_373t1:c.1931G>T	NP_612370.3:p.Gly644Val
XM_006717316.2:c.1832G>T	XP_006717379.1:p.Gly611Val
XM_006717316.4:c.1832G>T	XP_006717379.1:p.Gly611Val
XM_017015283.1:c.1931G>T	XP_016870772.1:p.Gly644Val
XM_017015284.2:c.1142G>T	XP_016870773.1:p.Gly381Val
XR_001746415.2:n.2466G>T
XR_929874.3:n.2290G>T
NM_001190723.3:c.1850G>T	NP_001177652.1:p.Gly617Val
NM_001005373.4:c.1931G>T MANE Select	NP_001005373.1:p.Gly644Val
NM_001005374.4:c.1931G>T	NP_001005374.1:p.Gly644Val
NM_001384142.1:c.1931G>T	NP_001371071.1:p.Gly644Val
NM_001384143.1:c.1832G>T	NP_001371072.1:p.Gly611Val
NM_001384144.1:c.1142G>T	NP_001371073.1:p.Gly381Val
NR_168891.1:n.2460G>T
NR_168892.1:n.2284G>T