Canonical Allele Identifier: CA374938136

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263298C>A (hg19) ; chr9:g.127501019C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501019C>A , CM000671.2:g.127501019C>A	GRCh38
NC_000009.11:g.130263298C>A , CM000671.1:g.130263298C>A	GRCh37
NC_000009.10:g.129303119C>A	NCBI36
NG_032008.1:g.54534C>A , LRG_373:g.54534C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1922C>A MANE Select	ENSP00000300417.6:p.Pro641Gln
ENST00000472068.2:c.*1646C>A	ENSP00000501555.1:n.*1646C>A
ENST00000483302.6:n.2587C>A
ENST00000498513.6:c.*813C>A	ENSP00000501637.1:n.*813C>A
ENST00000674511.1:n.1521C>A
ENST00000674516.1:c.*538C>A	ENSP00000502441.1:n.*538C>A
ENST00000674621.1:n.1861-2354C>A
ENST00000674771.1:c.*565C>A	ENSP00000502627.1:n.*565C>A
ENST00000674784.1:c.*982C>A	ENSP00000501837.1:n.*982C>A
ENST00000674970.1:c.*1696C>A	ENSP00000502493.1:n.*1696C>A
ENST00000675012.1:n.1866C>A
ENST00000675141.1:c.1823C>A	ENSP00000502420.1:p.Pro608Gln
ENST00000675198.1:n.1802C>A
ENST00000675213.1:c.1877C>A	ENSP00000502218.1:p.Pro626Gln
ENST00000675224.1:c.1950C>A	ENSP00000501869.1:p.Thr650=
ENST00000675253.1:c.*594C>A	ENSP00000502557.1:n.*594C>A
ENST00000675445.1:c.*1594C>A	ENSP00000502253.1:n.*1594C>A
ENST00000675448.1:c.1922C>A	ENSP00000502167.1:p.Pro641Gln
ENST00000675521.1:n.1832C>A
ENST00000675572.1:c.1823C>A	ENSP00000501598.1:p.Pro608Gln
ENST00000675641.1:c.*664C>A	ENSP00000501845.1:n.*664C>A
ENST00000675657.1:c.*535C>A	ENSP00000502002.1:n.*535C>A
ENST00000675662.1:n.1717C>A
ENST00000675789.1:c.1742C>A	ENSP00000501954.1:p.Pro581Gln
ENST00000675883.1:c.1841C>A	ENSP00000501592.1:p.Pro614Gln
ENST00000675945.1:c.*563C>A	ENSP00000501835.1:n.*563C>A
ENST00000676014.1:c.1865C>A	ENSP00000502058.1:p.Pro622Gln
ENST00000676035.1:n.1584C>A
ENST00000676106.1:n.1959C>A
ENST00000676137.1:n.1952C>A
ENST00000676170.1:c.2003C>A	ENSP00000502177.1:p.Pro668Gln
ENST00000676318.1:c.*2752C>A	ENSP00000502300.1:n.*2752C>A
ENST00000676336.1:c.*535C>A	ENSP00000502686.1:n.*535C>A
ENST00000676349.1:c.*1610C>A	ENSP00000502155.1:n.*1610C>A
ENST00000676399.1:n.1825C>A
ENST00000676409.1:n.1982C>A
ENST00000300417.10:c.1922C>A	ENSP00000300417.6:p.Pro641Gln
ENST00000323301.8:c.1922C>A	ENSP00000322937.4:p.Pro641Gln
ENST00000373322.1:c.1922C>A	ENSP00000362419.1:p.Pro641Gln
ENST00000373324.8:c.1841C>A	ENSP00000362421.4:p.Pro614Gln
ENST00000472068.1:n.815C>A
ENST00000483302.5:n.1144C>A
NM_001005373.3:c.1922C>A	NP_001005373.1:p.Pro641Gln
NM_001005374.3:c.1922C>A	NP_001005374.1:p.Pro641Gln
NM_001190723.2:c.1841C>A	NP_001177652.1:p.Pro614Gln
NM_138361.5:c.1922C>A , LRG_373t1:c.1922C>A	NP_612370.3:p.Pro641Gln
XM_006717316.2:c.1823C>A	XP_006717379.1:p.Pro608Gln
XM_006717316.4:c.1823C>A	XP_006717379.1:p.Pro608Gln
XM_017015283.1:c.1922C>A	XP_016870772.1:p.Pro641Gln
XM_017015284.2:c.1133C>A	XP_016870773.1:p.Pro378Gln
XR_001746415.2:n.2457C>A
XR_929874.3:n.2281C>A
NM_001190723.3:c.1841C>A	NP_001177652.1:p.Pro614Gln
NM_001005373.4:c.1922C>A MANE Select	NP_001005373.1:p.Pro641Gln
NM_001005374.4:c.1922C>A	NP_001005374.1:p.Pro641Gln
NM_001384142.1:c.1922C>A	NP_001371071.1:p.Pro641Gln
NM_001384143.1:c.1823C>A	NP_001371072.1:p.Pro608Gln
NM_001384144.1:c.1133C>A	NP_001371073.1:p.Pro378Gln
NR_168891.1:n.2451C>A
NR_168892.1:n.2275C>A