Canonical Allele Identifier: CA467236646

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263320C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501041C>A , CM000671.2:g.127501041C>A	GRCh38
NC_000009.11:g.130263320C>A , CM000671.1:g.130263320C>A	GRCh37
NC_000009.10:g.129303141C>A	NCBI36
NG_032008.1:g.54556C>A , LRG_373:g.54556C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1944C>A MANE Select	ENSP00000300417.6:p.Thr648=
ENST00000472068.2:c.*1668C>A	ENSP00000501555.1:n.*1668C>A
ENST00000483302.6:n.2609C>A
ENST00000498513.6:c.*835C>A	ENSP00000501637.1:n.*835C>A
ENST00000674511.1:n.1543C>A
ENST00000674516.1:c.*560C>A	ENSP00000502441.1:n.*560C>A
ENST00000674621.1:n.1861-2332C>A
ENST00000674771.1:c.*587C>A	ENSP00000502627.1:n.*587C>A
ENST00000674784.1:c.*1004C>A	ENSP00000501837.1:n.*1004C>A
ENST00000674970.1:c.*1718C>A	ENSP00000502493.1:n.*1718C>A
ENST00000675012.1:n.1888C>A
ENST00000675141.1:c.1845C>A	ENSP00000502420.1:p.Thr615=
ENST00000675198.1:n.1824C>A
ENST00000675213.1:c.1899C>A	ENSP00000502218.1:p.Thr633=
ENST00000675224.1:c.*10C>A	ENSP00000501869.1:n.*10C>A
ENST00000675253.1:c.*616C>A	ENSP00000502557.1:n.*616C>A
ENST00000675445.1:c.*1616C>A	ENSP00000502253.1:n.*1616C>A
ENST00000675448.1:c.1944C>A	ENSP00000502167.1:p.Thr648=
ENST00000675521.1:n.1854C>A
ENST00000675572.1:c.1845C>A	ENSP00000501598.1:p.Thr615=
ENST00000675641.1:c.*686C>A	ENSP00000501845.1:n.*686C>A
ENST00000675657.1:c.*557C>A	ENSP00000502002.1:n.*557C>A
ENST00000675662.1:n.1739C>A
ENST00000675789.1:c.1764C>A	ENSP00000501954.1:p.Thr588=
ENST00000675883.1:c.1863C>A	ENSP00000501592.1:p.Thr621=
ENST00000675945.1:c.*585C>A	ENSP00000501835.1:n.*585C>A
ENST00000676014.1:c.1887C>A	ENSP00000502058.1:p.Thr629=
ENST00000676035.1:n.1606C>A
ENST00000676106.1:n.1981C>A
ENST00000676137.1:n.1974C>A
ENST00000676170.1:c.2025C>A	ENSP00000502177.1:p.Thr675=
ENST00000676318.1:c.*2774C>A	ENSP00000502300.1:n.*2774C>A
ENST00000676336.1:c.*557C>A	ENSP00000502686.1:n.*557C>A
ENST00000676349.1:c.*1632C>A	ENSP00000502155.1:n.*1632C>A
ENST00000676399.1:n.1847C>A
ENST00000676409.1:n.2004C>A
ENST00000300417.10:c.1944C>A	ENSP00000300417.6:p.Thr648=
ENST00000323301.8:c.1944C>A	ENSP00000322937.4:p.Thr648=
ENST00000373322.1:c.1944C>A	ENSP00000362419.1:p.Thr648=
ENST00000373324.8:c.1863C>A	ENSP00000362421.4:p.Thr621=
ENST00000472068.1:n.837C>A
ENST00000483302.5:n.1166C>A
NM_001005373.3:c.1944C>A	NP_001005373.1:p.Thr648=
NM_001005374.3:c.1944C>A	NP_001005374.1:p.Thr648=
NM_001190723.2:c.1863C>A	NP_001177652.1:p.Thr621=
NM_138361.5:c.1944C>A , LRG_373t1:c.1944C>A	NP_612370.3:p.Thr648=
XM_006717316.2:c.1845C>A	XP_006717379.1:p.Thr615=
XM_006717316.4:c.1845C>A	XP_006717379.1:p.Thr615=
XM_017015283.1:c.1944C>A	XP_016870772.1:p.Thr648=
XM_017015284.2:c.1155C>A	XP_016870773.1:p.Thr385=
XR_001746415.2:n.2479C>A
XR_929874.3:n.2303C>A
NM_001190723.3:c.1863C>A	NP_001177652.1:p.Thr621=
NM_001005373.4:c.1944C>A MANE Select	NP_001005373.1:p.Thr648=
NM_001005374.4:c.1944C>A	NP_001005374.1:p.Thr648=
NM_001384142.1:c.1944C>A	NP_001371071.1:p.Thr648=
NM_001384143.1:c.1845C>A	NP_001371072.1:p.Thr615=
NM_001384144.1:c.1155C>A	NP_001371073.1:p.Thr385=
NR_168891.1:n.2473C>A
NR_168892.1:n.2297C>A