Canonical Allele Identifier: CA467233969

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127492879A>G , CM000671.2:g.127492879A>G	GRCh38
NC_000009.11:g.130255158A>G , CM000671.1:g.130255158A>G	GRCh37
NC_000009.10:g.129294979A>G	NCBI36
NG_032008.1:g.46394A>G , LRG_373:g.46394A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001005373.4:c.1581A>G MANE Select	NP_001005373.1:p.Glu527=
ENST00000300417.11:c.1581A>G MANE Select	ENSP00000300417.6:p.Glu527=
NM_001005373.3:c.1581A>G	NP_001005373.1:p.Glu527=
NM_001005374.3:c.1581A>G	NP_001005374.1:p.Glu527=
NM_001005374.4:c.1581A>G	NP_001005374.1:p.Glu527=
NM_001190723.2:c.1500A>G	NP_001177652.1:p.Glu500=
NM_001190723.3:c.1500A>G	NP_001177652.1:p.Glu500=
NM_001384142.1:c.1581A>G	NP_001371071.1:p.Glu527=
NM_001384143.1:c.1581A>G	NP_001371072.1:p.Glu527=
NM_001384144.1:c.792A>G	NP_001371073.1:p.Glu264=
NM_138361.5:c.1581A>G , LRG_373t1:c.1581A>G	NP_612370.3:p.Glu527=
NR_168891.1:n.2110A>G
NR_168892.1:n.1934A>G
ENST00000300417.10:c.1581A>G	ENSP00000300417.6:p.Glu527=
ENST00000323301.8:c.1581A>G	ENSP00000322937.4:p.Glu527=
ENST00000373322.1:c.1581A>G	ENSP00000362419.1:p.Glu527=
ENST00000373324.8:c.1500A>G	ENSP00000362421.4:p.Glu500=
ENST00000472068.1:n.573A>G
ENST00000472068.2:c.*1309A>G	ENSP00000501555.1:n.*1309A>G
ENST00000483302.5:n.803A>G
ENST00000483302.6:n.378A>G
ENST00000498513.6:c.*472A>G	ENSP00000501637.1:n.*472A>G
ENST00000674511.1:n.1298-3085A>G
ENST00000674516.1:c.1581A>G	ENSP00000502441.1:p.Glu527=
ENST00000674621.1:n.1631A>G
ENST00000674771.1:c.*323A>G	ENSP00000502627.1:n.*323A>G
ENST00000674784.1:c.*740A>G	ENSP00000501837.1:n.*740A>G
ENST00000674970.1:c.*1355A>G	ENSP00000502493.1:n.*1355A>G
ENST00000675012.1:n.1525A>G
ENST00000675141.1:c.1581A>G	ENSP00000502420.1:p.Glu527=
ENST00000675198.1:n.1461A>G
ENST00000675213.1:c.1536A>G	ENSP00000502218.1:p.Glu512=
ENST00000675224.1:c.1581A>G	ENSP00000501869.1:p.Glu527=
ENST00000675253.1:c.*352A>G	ENSP00000502557.1:n.*352A>G
ENST00000675445.1:c.*1253A>G	ENSP00000502253.1:n.*1253A>G
ENST00000675448.1:c.1581A>G	ENSP00000502167.1:p.Glu527=
ENST00000675521.1:n.1491A>G
ENST00000675572.1:c.1581A>G	ENSP00000501598.1:p.Glu527=
ENST00000675641.1:c.*323A>G	ENSP00000501845.1:n.*323A>G
ENST00000675657.1:c.*194A>G	ENSP00000502002.1:n.*194A>G
ENST00000675662.1:n.1376A>G
ENST00000675789.1:c.1500A>G	ENSP00000501954.1:p.Glu500=
ENST00000675883.1:c.1500A>G	ENSP00000501592.1:p.Glu500=
ENST00000675945.1:c.*403A>G	ENSP00000501835.1:n.*403A>G
ENST00000676014.1:c.1524A>G	ENSP00000502058.1:p.Glu508=
ENST00000676035.1:n.1342A>G
ENST00000676106.1:n.1386A>G
ENST00000676137.1:n.1611A>G
ENST00000676170.1:c.1662A>G	ENSP00000502177.1:p.Glu554=
ENST00000676318.1:c.*323A>G	ENSP00000502300.1:n.*323A>G
ENST00000676336.1:c.*194A>G	ENSP00000502686.1:n.*194A>G
ENST00000676349.1:c.*1269A>G	ENSP00000502155.1:n.*1269A>G
ENST00000676399.1:n.1484A>G
ENST00000676409.1:n.1641A>G
XM_006717316.2:c.1581A>G	XP_006717379.1:p.Glu527=
XM_006717316.4:c.1581A>G	XP_006717379.1:p.Glu527=
XM_017015283.1:c.1581A>G	XP_016870772.1:p.Glu527=
XM_017015284.2:c.792A>G	XP_016870773.1:p.Glu264=
XR_001746415.2:n.2116A>G
XR_929874.3:n.1940A>G