Canonical Allele Identifier: CA374938132

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263297C>A (hg19) ; chr9:g.127501018C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501018C>A , CM000671.2:g.127501018C>A	GRCh38
NC_000009.11:g.130263297C>A , CM000671.1:g.130263297C>A	GRCh37
NC_000009.10:g.129303118C>A	NCBI36
NG_032008.1:g.54533C>A , LRG_373:g.54533C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1921C>A MANE Select	ENSP00000300417.6:p.Pro641Thr
ENST00000472068.2:c.*1645C>A	ENSP00000501555.1:n.*1645C>A
ENST00000483302.6:n.2586C>A
ENST00000498513.6:c.*812C>A	ENSP00000501637.1:n.*812C>A
ENST00000674511.1:n.1520C>A
ENST00000674516.1:c.*537C>A	ENSP00000502441.1:n.*537C>A
ENST00000674621.1:n.1861-2355C>A
ENST00000674771.1:c.*564C>A	ENSP00000502627.1:n.*564C>A
ENST00000674784.1:c.*981C>A	ENSP00000501837.1:n.*981C>A
ENST00000674970.1:c.*1695C>A	ENSP00000502493.1:n.*1695C>A
ENST00000675012.1:n.1865C>A
ENST00000675141.1:c.1822C>A	ENSP00000502420.1:p.Pro608Thr
ENST00000675198.1:n.1801C>A
ENST00000675213.1:c.1876C>A	ENSP00000502218.1:p.Pro626Thr
ENST00000675224.1:c.1949C>A	ENSP00000501869.1:p.Thr650Asn
ENST00000675253.1:c.*593C>A	ENSP00000502557.1:n.*593C>A
ENST00000675445.1:c.*1593C>A	ENSP00000502253.1:n.*1593C>A
ENST00000675448.1:c.1921C>A	ENSP00000502167.1:p.Pro641Thr
ENST00000675521.1:n.1831C>A
ENST00000675572.1:c.1822C>A	ENSP00000501598.1:p.Pro608Thr
ENST00000675641.1:c.*663C>A	ENSP00000501845.1:n.*663C>A
ENST00000675657.1:c.*534C>A	ENSP00000502002.1:n.*534C>A
ENST00000675662.1:n.1716C>A
ENST00000675789.1:c.1741C>A	ENSP00000501954.1:p.Pro581Thr
ENST00000675883.1:c.1840C>A	ENSP00000501592.1:p.Pro614Thr
ENST00000675945.1:c.*562C>A	ENSP00000501835.1:n.*562C>A
ENST00000676014.1:c.1864C>A	ENSP00000502058.1:p.Pro622Thr
ENST00000676035.1:n.1583C>A
ENST00000676106.1:n.1958C>A
ENST00000676137.1:n.1951C>A
ENST00000676170.1:c.2002C>A	ENSP00000502177.1:p.Pro668Thr
ENST00000676318.1:c.*2751C>A	ENSP00000502300.1:n.*2751C>A
ENST00000676336.1:c.*534C>A	ENSP00000502686.1:n.*534C>A
ENST00000676349.1:c.*1609C>A	ENSP00000502155.1:n.*1609C>A
ENST00000676399.1:n.1824C>A
ENST00000676409.1:n.1981C>A
ENST00000300417.10:c.1921C>A	ENSP00000300417.6:p.Pro641Thr
ENST00000323301.8:c.1921C>A	ENSP00000322937.4:p.Pro641Thr
ENST00000373322.1:c.1921C>A	ENSP00000362419.1:p.Pro641Thr
ENST00000373324.8:c.1840C>A	ENSP00000362421.4:p.Pro614Thr
ENST00000472068.1:n.814C>A
ENST00000483302.5:n.1143C>A
NM_001005373.3:c.1921C>A	NP_001005373.1:p.Pro641Thr
NM_001005374.3:c.1921C>A	NP_001005374.1:p.Pro641Thr
NM_001190723.2:c.1840C>A	NP_001177652.1:p.Pro614Thr
NM_138361.5:c.1921C>A , LRG_373t1:c.1921C>A	NP_612370.3:p.Pro641Thr
XM_006717316.2:c.1822C>A	XP_006717379.1:p.Pro608Thr
XM_006717316.4:c.1822C>A	XP_006717379.1:p.Pro608Thr
XM_017015283.1:c.1921C>A	XP_016870772.1:p.Pro641Thr
XM_017015284.2:c.1132C>A	XP_016870773.1:p.Pro378Thr
XR_001746415.2:n.2456C>A
XR_929874.3:n.2280C>A
NM_001190723.3:c.1840C>A	NP_001177652.1:p.Pro614Thr
NM_001005373.4:c.1921C>A MANE Select	NP_001005373.1:p.Pro641Thr
NM_001005374.4:c.1921C>A	NP_001005374.1:p.Pro641Thr
NM_001384142.1:c.1921C>A	NP_001371071.1:p.Pro641Thr
NM_001384143.1:c.1822C>A	NP_001371072.1:p.Pro608Thr
NM_001384144.1:c.1132C>A	NP_001371073.1:p.Pro378Thr
NR_168891.1:n.2450C>A
NR_168892.1:n.2274C>A