Canonical Allele Identifier: CA467236813

Gene: LRSAM1

Linked Data

• gnomAD v4: 9-127501086-T-A
• MyVariant Identifiers: chr9:g.130263365T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501086T>A , CM000671.2:g.127501086T>A	GRCh38
NC_000009.11:g.130263365T>A , CM000671.1:g.130263365T>A	GRCh37
NC_000009.10:g.129303186T>A	NCBI36
NG_032008.1:g.54601T>A , LRG_373:g.54601T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1989T>A MANE Select	ENSP00000300417.6:p.Ala663=
ENST00000472068.2:c.*1713T>A	ENSP00000501555.1:n.*1713T>A
ENST00000483302.6:n.2654T>A
ENST00000498513.6:c.*880T>A	ENSP00000501637.1:n.*880T>A
ENST00000674511.1:n.1588T>A
ENST00000674516.1:c.*605T>A	ENSP00000502441.1:n.*605T>A
ENST00000674621.1:n.1861-2287T>A
ENST00000674771.1:c.*632T>A	ENSP00000502627.1:n.*632T>A
ENST00000674784.1:c.*1049T>A	ENSP00000501837.1:n.*1049T>A
ENST00000674970.1:c.*1763T>A	ENSP00000502493.1:n.*1763T>A
ENST00000675012.1:n.1933T>A
ENST00000675141.1:c.1890T>A	ENSP00000502420.1:p.Ala630=
ENST00000675198.1:n.1869T>A
ENST00000675213.1:c.1944T>A	ENSP00000502218.1:p.Ala648=
ENST00000675224.1:c.*55T>A	ENSP00000501869.1:n.*55T>A
ENST00000675253.1:c.*661T>A	ENSP00000502557.1:n.*661T>A
ENST00000675445.1:c.*1661T>A	ENSP00000502253.1:n.*1661T>A
ENST00000675448.1:c.1989T>A	ENSP00000502167.1:p.Ala663=
ENST00000675521.1:n.1899T>A
ENST00000675572.1:c.1890T>A	ENSP00000501598.1:p.Ala630=
ENST00000675641.1:c.*731T>A	ENSP00000501845.1:n.*731T>A
ENST00000675657.1:c.*602T>A	ENSP00000502002.1:n.*602T>A
ENST00000675662.1:n.1784T>A
ENST00000675789.1:c.1809T>A	ENSP00000501954.1:p.Ala603=
ENST00000675883.1:c.1908T>A	ENSP00000501592.1:p.Ala636=
ENST00000675945.1:c.*630T>A	ENSP00000501835.1:n.*630T>A
ENST00000676014.1:c.1932T>A	ENSP00000502058.1:p.Ala644=
ENST00000676035.1:n.1651T>A
ENST00000676106.1:n.2026T>A
ENST00000676137.1:n.2019T>A
ENST00000676170.1:c.2070T>A	ENSP00000502177.1:p.Ala690=
ENST00000676318.1:c.*2819T>A	ENSP00000502300.1:n.*2819T>A
ENST00000676336.1:c.*602T>A	ENSP00000502686.1:n.*602T>A
ENST00000676349.1:c.*1677T>A	ENSP00000502155.1:n.*1677T>A
ENST00000676399.1:n.1892T>A
ENST00000676409.1:n.2049T>A
ENST00000300417.10:c.1989T>A	ENSP00000300417.6:p.Ala663=
ENST00000323301.8:c.1989T>A	ENSP00000322937.4:p.Ala663=
ENST00000373322.1:c.1989T>A	ENSP00000362419.1:p.Ala663=
ENST00000373324.8:c.1908T>A	ENSP00000362421.4:p.Ala636=
ENST00000483302.5:n.1211T>A
NM_001005373.3:c.1989T>A	NP_001005373.1:p.Ala663=
NM_001005374.3:c.1989T>A	NP_001005374.1:p.Ala663=
NM_001190723.2:c.1908T>A	NP_001177652.1:p.Ala636=
NM_138361.5:c.1989T>A , LRG_373t1:c.1989T>A	NP_612370.3:p.Ala663=
XM_006717316.2:c.1890T>A	XP_006717379.1:p.Ala630=
XM_006717316.4:c.1890T>A	XP_006717379.1:p.Ala630=
XM_017015283.1:c.1989T>A	XP_016870772.1:p.Ala663=
XM_017015284.2:c.1200T>A	XP_016870773.1:p.Ala400=
XR_001746415.2:n.2524T>A
XR_929874.3:n.2348T>A
NM_001190723.3:c.1908T>A	NP_001177652.1:p.Ala636=
NM_001005373.4:c.1989T>A MANE Select	NP_001005373.1:p.Ala663=
NM_001005374.4:c.1989T>A	NP_001005374.1:p.Ala663=
NM_001384142.1:c.1989T>A	NP_001371071.1:p.Ala663=
NM_001384143.1:c.1890T>A	NP_001371072.1:p.Ala630=
NM_001384144.1:c.1200T>A	NP_001371073.1:p.Ala400=
NR_168891.1:n.2518T>A
NR_168892.1:n.2342T>A