Canonical Allele Identifier: CA374938241

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263352T>A (hg19) ; chr9:g.127501073T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501073T>A , CM000671.2:g.127501073T>A	GRCh38
NC_000009.11:g.130263352T>A , CM000671.1:g.130263352T>A	GRCh37
NC_000009.10:g.129303173T>A	NCBI36
NG_032008.1:g.54588T>A , LRG_373:g.54588T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1976T>A MANE Select	ENSP00000300417.6:p.Val659Glu
ENST00000472068.2:c.*1700T>A	ENSP00000501555.1:n.*1700T>A
ENST00000483302.6:n.2641T>A
ENST00000498513.6:c.*867T>A	ENSP00000501637.1:n.*867T>A
ENST00000674511.1:n.1575T>A
ENST00000674516.1:c.*592T>A	ENSP00000502441.1:n.*592T>A
ENST00000674621.1:n.1861-2300T>A
ENST00000674771.1:c.*619T>A	ENSP00000502627.1:n.*619T>A
ENST00000674784.1:c.*1036T>A	ENSP00000501837.1:n.*1036T>A
ENST00000674970.1:c.*1750T>A	ENSP00000502493.1:n.*1750T>A
ENST00000675012.1:n.1920T>A
ENST00000675141.1:c.1877T>A	ENSP00000502420.1:p.Val626Glu
ENST00000675198.1:n.1856T>A
ENST00000675213.1:c.1931T>A	ENSP00000502218.1:p.Val644Glu
ENST00000675224.1:c.*42T>A	ENSP00000501869.1:n.*42T>A
ENST00000675253.1:c.*648T>A	ENSP00000502557.1:n.*648T>A
ENST00000675445.1:c.*1648T>A	ENSP00000502253.1:n.*1648T>A
ENST00000675448.1:c.1976T>A	ENSP00000502167.1:p.Val659Glu
ENST00000675521.1:n.1886T>A
ENST00000675572.1:c.1877T>A	ENSP00000501598.1:p.Val626Glu
ENST00000675641.1:c.*718T>A	ENSP00000501845.1:n.*718T>A
ENST00000675657.1:c.*589T>A	ENSP00000502002.1:n.*589T>A
ENST00000675662.1:n.1771T>A
ENST00000675789.1:c.1796T>A	ENSP00000501954.1:p.Val599Glu
ENST00000675883.1:c.1895T>A	ENSP00000501592.1:p.Val632Glu
ENST00000675945.1:c.*617T>A	ENSP00000501835.1:n.*617T>A
ENST00000676014.1:c.1919T>A	ENSP00000502058.1:p.Val640Glu
ENST00000676035.1:n.1638T>A
ENST00000676106.1:n.2013T>A
ENST00000676137.1:n.2006T>A
ENST00000676170.1:c.2057T>A	ENSP00000502177.1:p.Val686Glu
ENST00000676318.1:c.*2806T>A	ENSP00000502300.1:n.*2806T>A
ENST00000676336.1:c.*589T>A	ENSP00000502686.1:n.*589T>A
ENST00000676349.1:c.*1664T>A	ENSP00000502155.1:n.*1664T>A
ENST00000676399.1:n.1879T>A
ENST00000676409.1:n.2036T>A
ENST00000300417.10:c.1976T>A	ENSP00000300417.6:p.Val659Glu
ENST00000323301.8:c.1976T>A	ENSP00000322937.4:p.Val659Glu
ENST00000373322.1:c.1976T>A	ENSP00000362419.1:p.Val659Glu
ENST00000373324.8:c.1895T>A	ENSP00000362421.4:p.Val632Glu
ENST00000483302.5:n.1198T>A
NM_001005373.3:c.1976T>A	NP_001005373.1:p.Val659Glu
NM_001005374.3:c.1976T>A	NP_001005374.1:p.Val659Glu
NM_001190723.2:c.1895T>A	NP_001177652.1:p.Val632Glu
NM_138361.5:c.1976T>A , LRG_373t1:c.1976T>A	NP_612370.3:p.Val659Glu
XM_006717316.2:c.1877T>A	XP_006717379.1:p.Val626Glu
XM_006717316.4:c.1877T>A	XP_006717379.1:p.Val626Glu
XM_017015283.1:c.1976T>A	XP_016870772.1:p.Val659Glu
XM_017015284.2:c.1187T>A	XP_016870773.1:p.Val396Glu
XR_001746415.2:n.2511T>A
XR_929874.3:n.2335T>A
NM_001190723.3:c.1895T>A	NP_001177652.1:p.Val632Glu
NM_001005373.4:c.1976T>A MANE Select	NP_001005373.1:p.Val659Glu
NM_001005374.4:c.1976T>A	NP_001005374.1:p.Val659Glu
NM_001384142.1:c.1976T>A	NP_001371071.1:p.Val659Glu
NM_001384143.1:c.1877T>A	NP_001371072.1:p.Val626Glu
NM_001384144.1:c.1187T>A	NP_001371073.1:p.Val396Glu
NR_168891.1:n.2505T>A
NR_168892.1:n.2329T>A