Canonical Allele Identifier: CA374938256

Gene: LRSAM1

Linked Data

• gnomAD v4: 9-127501081-T-C
• MyVariant Identifiers: chr9:g.130263360T>C (hg19) ; chr9:g.127501081T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501081T>C , CM000671.2:g.127501081T>C	GRCh38
NC_000009.11:g.130263360T>C , CM000671.1:g.130263360T>C	GRCh37
NC_000009.10:g.129303181T>C	NCBI36
NG_032008.1:g.54596T>C , LRG_373:g.54596T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1984T>C MANE Select	ENSP00000300417.6:p.Ser662Pro
ENST00000472068.2:c.*1708T>C	ENSP00000501555.1:n.*1708T>C
ENST00000483302.6:n.2649T>C
ENST00000498513.6:c.*875T>C	ENSP00000501637.1:n.*875T>C
ENST00000674511.1:n.1583T>C
ENST00000674516.1:c.*600T>C	ENSP00000502441.1:n.*600T>C
ENST00000674621.1:n.1861-2292T>C
ENST00000674771.1:c.*627T>C	ENSP00000502627.1:n.*627T>C
ENST00000674784.1:c.*1044T>C	ENSP00000501837.1:n.*1044T>C
ENST00000674970.1:c.*1758T>C	ENSP00000502493.1:n.*1758T>C
ENST00000675012.1:n.1928T>C
ENST00000675141.1:c.1885T>C	ENSP00000502420.1:p.Ser629Pro
ENST00000675198.1:n.1864T>C
ENST00000675213.1:c.1939T>C	ENSP00000502218.1:p.Ser647Pro
ENST00000675224.1:c.*50T>C	ENSP00000501869.1:n.*50T>C
ENST00000675253.1:c.*656T>C	ENSP00000502557.1:n.*656T>C
ENST00000675445.1:c.*1656T>C	ENSP00000502253.1:n.*1656T>C
ENST00000675448.1:c.1984T>C	ENSP00000502167.1:p.Ser662Pro
ENST00000675521.1:n.1894T>C
ENST00000675572.1:c.1885T>C	ENSP00000501598.1:p.Ser629Pro
ENST00000675641.1:c.*726T>C	ENSP00000501845.1:n.*726T>C
ENST00000675657.1:c.*597T>C	ENSP00000502002.1:n.*597T>C
ENST00000675662.1:n.1779T>C
ENST00000675789.1:c.1804T>C	ENSP00000501954.1:p.Ser602Pro
ENST00000675883.1:c.1903T>C	ENSP00000501592.1:p.Ser635Pro
ENST00000675945.1:c.*625T>C	ENSP00000501835.1:n.*625T>C
ENST00000676014.1:c.1927T>C	ENSP00000502058.1:p.Ser643Pro
ENST00000676035.1:n.1646T>C
ENST00000676106.1:n.2021T>C
ENST00000676137.1:n.2014T>C
ENST00000676170.1:c.2065T>C	ENSP00000502177.1:p.Ser689Pro
ENST00000676318.1:c.*2814T>C	ENSP00000502300.1:n.*2814T>C
ENST00000676336.1:c.*597T>C	ENSP00000502686.1:n.*597T>C
ENST00000676349.1:c.*1672T>C	ENSP00000502155.1:n.*1672T>C
ENST00000676399.1:n.1887T>C
ENST00000676409.1:n.2044T>C
ENST00000300417.10:c.1984T>C	ENSP00000300417.6:p.Ser662Pro
ENST00000323301.8:c.1984T>C	ENSP00000322937.4:p.Ser662Pro
ENST00000373322.1:c.1984T>C	ENSP00000362419.1:p.Ser662Pro
ENST00000373324.8:c.1903T>C	ENSP00000362421.4:p.Ser635Pro
ENST00000483302.5:n.1206T>C
NM_001005373.3:c.1984T>C	NP_001005373.1:p.Ser662Pro
NM_001005374.3:c.1984T>C	NP_001005374.1:p.Ser662Pro
NM_001190723.2:c.1903T>C	NP_001177652.1:p.Ser635Pro
NM_138361.5:c.1984T>C , LRG_373t1:c.1984T>C	NP_612370.3:p.Ser662Pro
XM_006717316.2:c.1885T>C	XP_006717379.1:p.Ser629Pro
XM_006717316.4:c.1885T>C	XP_006717379.1:p.Ser629Pro
XM_017015283.1:c.1984T>C	XP_016870772.1:p.Ser662Pro
XM_017015284.2:c.1195T>C	XP_016870773.1:p.Ser399Pro
XR_001746415.2:n.2519T>C
XR_929874.3:n.2343T>C
NM_001190723.3:c.1903T>C	NP_001177652.1:p.Ser635Pro
NM_001005373.4:c.1984T>C MANE Select	NP_001005373.1:p.Ser662Pro
NM_001005374.4:c.1984T>C	NP_001005374.1:p.Ser662Pro
NM_001384142.1:c.1984T>C	NP_001371071.1:p.Ser662Pro
NM_001384143.1:c.1885T>C	NP_001371072.1:p.Ser629Pro
NM_001384144.1:c.1195T>C	NP_001371073.1:p.Ser399Pro
NR_168891.1:n.2513T>C
NR_168892.1:n.2337T>C