Canonical Allele Identifier: CA1879828755

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501103_127501104delinsAG , CM000671.2:g.127501103_127501104delinsAG	GRCh38
NC_000009.11:g.130263382_130263383delinsAG , CM000671.1:g.130263382_130263383delinsAG	GRCh37
NC_000009.10:g.129303203_129303204delinsAG	NCBI36
NG_032008.1:g.54618_54619delinsAG , LRG_373:g.54618_54619delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2006_2007delinsAG MANE Select	ENSP00000300417.6:p.Glu669=
ENST00000472068.2:c.*1730_*1731delinsAG	ENSP00000501555.1:n.*1730_*1731delinsAG
ENST00000483302.6:n.2671_2672delinsAG
ENST00000498513.6:c.*897_*898delinsAG	ENSP00000501637.1:n.*897_*898delinsAG
ENST00000674511.1:n.1605_1606delinsAG
ENST00000674516.1:c.*622_*623delinsAG	ENSP00000502441.1:n.*622_*623delinsAG
ENST00000674621.1:n.1861-2270_1861-2269delinsAG
ENST00000674771.1:c.*649_*650delinsAG	ENSP00000502627.1:n.*649_*650delinsAG
ENST00000674784.1:c.*1066_*1067delinsAG	ENSP00000501837.1:n.*1066_*1067delinsAG
ENST00000674970.1:c.*1780_*1781delinsAG	ENSP00000502493.1:n.*1780_*1781delinsAG
ENST00000675012.1:n.1950_1951delinsAG
ENST00000675141.1:c.1907_1908delinsAG	ENSP00000502420.1:p.Glu636=
ENST00000675198.1:n.1886_1887delinsAG
ENST00000675213.1:c.1961_1962delinsAG	ENSP00000502218.1:p.Glu654=
ENST00000675224.1:c.*72_*73delinsAG	ENSP00000501869.1:n.*72_*73delinsAG
ENST00000675253.1:c.*678_*679delinsAG	ENSP00000502557.1:n.*678_*679delinsAG
ENST00000675445.1:c.*1678_*1679delinsAG	ENSP00000502253.1:n.*1678_*1679delinsAG
ENST00000675448.1:c.2006_2007delinsAG	ENSP00000502167.1:p.Glu669=
ENST00000675521.1:n.1916_1917delinsAG
ENST00000675572.1:c.1907_1908delinsAG	ENSP00000501598.1:p.Glu636=
ENST00000675641.1:c.*748_*749delinsAG	ENSP00000501845.1:n.*748_*749delinsAG
ENST00000675657.1:c.*619_*620delinsAG	ENSP00000502002.1:n.*619_*620delinsAG
ENST00000675662.1:n.1801_1802delinsAG
ENST00000675789.1:c.1826_1827delinsAG	ENSP00000501954.1:p.Glu609=
ENST00000675883.1:c.1925_1926delinsAG	ENSP00000501592.1:p.Glu642=
ENST00000675945.1:c.*647_*648delinsAG	ENSP00000501835.1:n.*647_*648delinsAG
ENST00000676014.1:c.1949_1950delinsAG	ENSP00000502058.1:p.Glu650=
ENST00000676035.1:n.1668_1669delinsAG
ENST00000676106.1:n.2043_2044delinsAG
ENST00000676137.1:n.2036_2037delinsAG
ENST00000676170.1:c.2087_2088delinsAG	ENSP00000502177.1:p.Glu696=
ENST00000676318.1:c.*2836_*2837delinsAG	ENSP00000502300.1:n.*2836_*2837delinsAG
ENST00000676336.1:c.*619_*620delinsAG	ENSP00000502686.1:n.*619_*620delinsAG
ENST00000676349.1:c.*1694_*1695delinsAG	ENSP00000502155.1:n.*1694_*1695delinsAG
ENST00000676399.1:n.1909_1910delinsAG
ENST00000676409.1:n.2066_2067delinsAG
ENST00000300417.10:c.2006_2007delinsAG	ENSP00000300417.6:p.Glu669=
ENST00000323301.8:c.2006_2007delinsAG	ENSP00000322937.4:p.Glu669=
ENST00000373322.1:c.2006_2007delinsAG	ENSP00000362419.1:p.Glu669=
ENST00000373324.8:c.1925_1926delinsAG	ENSP00000362421.4:p.Glu642=
ENST00000483302.5:n.1228_1229delinsAG
NM_001005373.3:c.2006_2007delinsAG	NP_001005373.1:p.Glu669=
NM_001005374.3:c.2006_2007delinsAG	NP_001005374.1:p.Glu669=
NM_001190723.2:c.1925_1926delinsAG	NP_001177652.1:p.Glu642=
NM_138361.5:c.2006_2007delinsAG , LRG_373t1:c.2006_2007delinsAG	NP_612370.3:p.Glu669=
XM_006717316.2:c.1907_1908delinsAG	XP_006717379.1:p.Glu636=
XM_006717316.4:c.1907_1908delinsAG	XP_006717379.1:p.Glu636=
XM_017015283.1:c.2006_2007delinsAG	XP_016870772.1:p.Glu669=
XM_017015284.2:c.1217_1218delinsAG	XP_016870773.1:p.Glu406=
XR_001746415.2:n.2541_2542delinsAG
XR_929874.3:n.2365_2366delinsAG
NM_001190723.3:c.1925_1926delinsAG	NP_001177652.1:p.Glu642=
NM_001005373.4:c.2006_2007delinsAG MANE Select	NP_001005373.1:p.Glu669=
NM_001005374.4:c.2006_2007delinsAG	NP_001005374.1:p.Glu669=
NM_001384142.1:c.2006_2007delinsAG	NP_001371071.1:p.Glu669=
NM_001384143.1:c.1907_1908delinsAG	NP_001371072.1:p.Glu636=
NM_001384144.1:c.1217_1218delinsAG	NP_001371073.1:p.Glu406=
NR_168891.1:n.2535_2536delinsAG
NR_168892.1:n.2359_2360delinsAG