Canonical Allele Identifier: CA374938129

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263295A>G (hg19) ; chr9:g.127501016A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501016A>G , CM000671.2:g.127501016A>G	GRCh38
NC_000009.11:g.130263295A>G , CM000671.1:g.130263295A>G	GRCh37
NC_000009.10:g.129303116A>G	NCBI36
NG_032008.1:g.54531A>G , LRG_373:g.54531A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1919A>G MANE Select	ENSP00000300417.6:p.Lys640Arg
ENST00000472068.2:c.*1643A>G	ENSP00000501555.1:n.*1643A>G
ENST00000483302.6:n.2584A>G
ENST00000498513.6:c.*810A>G	ENSP00000501637.1:n.*810A>G
ENST00000674511.1:n.1518A>G
ENST00000674516.1:c.*535A>G	ENSP00000502441.1:n.*535A>G
ENST00000674621.1:n.1861-2357A>G
ENST00000674771.1:c.*562A>G	ENSP00000502627.1:n.*562A>G
ENST00000674784.1:c.*979A>G	ENSP00000501837.1:n.*979A>G
ENST00000674970.1:c.*1693A>G	ENSP00000502493.1:n.*1693A>G
ENST00000675012.1:n.1863A>G
ENST00000675141.1:c.1820A>G	ENSP00000502420.1:p.Lys607Arg
ENST00000675198.1:n.1799A>G
ENST00000675213.1:c.1874A>G	ENSP00000502218.1:p.Lys625Arg
ENST00000675224.1:c.1947A>G	ENSP00000501869.1:p.Glu649=
ENST00000675253.1:c.*591A>G	ENSP00000502557.1:n.*591A>G
ENST00000675445.1:c.*1591A>G	ENSP00000502253.1:n.*1591A>G
ENST00000675448.1:c.1919A>G	ENSP00000502167.1:p.Lys640Arg
ENST00000675521.1:n.1829A>G
ENST00000675572.1:c.1820A>G	ENSP00000501598.1:p.Lys607Arg
ENST00000675641.1:c.*661A>G	ENSP00000501845.1:n.*661A>G
ENST00000675657.1:c.*532A>G	ENSP00000502002.1:n.*532A>G
ENST00000675662.1:n.1714A>G
ENST00000675789.1:c.1739A>G	ENSP00000501954.1:p.Lys580Arg
ENST00000675883.1:c.1838A>G	ENSP00000501592.1:p.Lys613Arg
ENST00000675945.1:c.*560A>G	ENSP00000501835.1:n.*560A>G
ENST00000676014.1:c.1862A>G	ENSP00000502058.1:p.Lys621Arg
ENST00000676035.1:n.1581A>G
ENST00000676106.1:n.1956A>G
ENST00000676137.1:n.1949A>G
ENST00000676170.1:c.2000A>G	ENSP00000502177.1:p.Lys667Arg
ENST00000676318.1:c.*2749A>G	ENSP00000502300.1:n.*2749A>G
ENST00000676336.1:c.*532A>G	ENSP00000502686.1:n.*532A>G
ENST00000676349.1:c.*1607A>G	ENSP00000502155.1:n.*1607A>G
ENST00000676399.1:n.1822A>G
ENST00000676409.1:n.1979A>G
ENST00000300417.10:c.1919A>G	ENSP00000300417.6:p.Lys640Arg
ENST00000323301.8:c.1919A>G	ENSP00000322937.4:p.Lys640Arg
ENST00000373322.1:c.1919A>G	ENSP00000362419.1:p.Lys640Arg
ENST00000373324.8:c.1838A>G	ENSP00000362421.4:p.Lys613Arg
ENST00000472068.1:n.812A>G
ENST00000483302.5:n.1141A>G
NM_001005373.3:c.1919A>G	NP_001005373.1:p.Lys640Arg
NM_001005374.3:c.1919A>G	NP_001005374.1:p.Lys640Arg
NM_001190723.2:c.1838A>G	NP_001177652.1:p.Lys613Arg
NM_138361.5:c.1919A>G , LRG_373t1:c.1919A>G	NP_612370.3:p.Lys640Arg
XM_006717316.2:c.1820A>G	XP_006717379.1:p.Lys607Arg
XM_006717316.4:c.1820A>G	XP_006717379.1:p.Lys607Arg
XM_017015283.1:c.1919A>G	XP_016870772.1:p.Lys640Arg
XM_017015284.2:c.1130A>G	XP_016870773.1:p.Lys377Arg
XR_001746415.2:n.2454A>G
XR_929874.3:n.2278A>G
NM_001190723.3:c.1838A>G	NP_001177652.1:p.Lys613Arg
NM_001005373.4:c.1919A>G MANE Select	NP_001005373.1:p.Lys640Arg
NM_001005374.4:c.1919A>G	NP_001005374.1:p.Lys640Arg
NM_001384142.1:c.1919A>G	NP_001371071.1:p.Lys640Arg
NM_001384143.1:c.1820A>G	NP_001371072.1:p.Lys607Arg
NM_001384144.1:c.1130A>G	NP_001371073.1:p.Lys377Arg
NR_168891.1:n.2448A>G
NR_168892.1:n.2272A>G