Canonical Allele Identifier: CA374938318

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263394C>A (hg19) ; chr9:g.127501115C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501115C>A , CM000671.2:g.127501115C>A	GRCh38
NC_000009.11:g.130263394C>A , CM000671.1:g.130263394C>A	GRCh37
NC_000009.10:g.129303215C>A	NCBI36
NG_032008.1:g.54630C>A , LRG_373:g.54630C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2018C>A MANE Select	ENSP00000300417.6:p.Ser673Ter
ENST00000472068.2:c.*1742C>A	ENSP00000501555.1:n.*1742C>A
ENST00000483302.6:n.2683C>A
ENST00000498513.6:c.*909C>A	ENSP00000501637.1:n.*909C>A
ENST00000674511.1:n.1617C>A
ENST00000674516.1:c.*634C>A	ENSP00000502441.1:n.*634C>A
ENST00000674621.1:n.1861-2258C>A
ENST00000674771.1:c.*661C>A	ENSP00000502627.1:n.*661C>A
ENST00000674784.1:c.*1078C>A	ENSP00000501837.1:n.*1078C>A
ENST00000674970.1:c.*1792C>A	ENSP00000502493.1:n.*1792C>A
ENST00000675012.1:n.1962C>A
ENST00000675141.1:c.1919C>A	ENSP00000502420.1:p.Ser640Ter
ENST00000675198.1:n.1898C>A
ENST00000675213.1:c.1973C>A	ENSP00000502218.1:p.Ser658Ter
ENST00000675224.1:c.*84C>A	ENSP00000501869.1:n.*84C>A
ENST00000675253.1:c.*690C>A	ENSP00000502557.1:n.*690C>A
ENST00000675445.1:c.*1690C>A	ENSP00000502253.1:n.*1690C>A
ENST00000675448.1:c.2018C>A	ENSP00000502167.1:p.Ser673Ter
ENST00000675521.1:n.1928C>A
ENST00000675572.1:c.1919C>A	ENSP00000501598.1:p.Ser640Ter
ENST00000675641.1:c.*760C>A	ENSP00000501845.1:n.*760C>A
ENST00000675657.1:c.*631C>A	ENSP00000502002.1:n.*631C>A
ENST00000675662.1:n.1813C>A
ENST00000675789.1:c.1838C>A	ENSP00000501954.1:p.Ser613Ter
ENST00000675883.1:c.1937C>A	ENSP00000501592.1:p.Ser646Ter
ENST00000675945.1:c.*659C>A	ENSP00000501835.1:n.*659C>A
ENST00000676014.1:c.1961C>A	ENSP00000502058.1:p.Ser654Ter
ENST00000676035.1:n.1680C>A
ENST00000676106.1:n.2055C>A
ENST00000676137.1:n.2048C>A
ENST00000676170.1:c.2099C>A	ENSP00000502177.1:p.Ser700Ter
ENST00000676318.1:c.*2848C>A	ENSP00000502300.1:n.*2848C>A
ENST00000676336.1:c.*631C>A	ENSP00000502686.1:n.*631C>A
ENST00000676349.1:c.*1706C>A	ENSP00000502155.1:n.*1706C>A
ENST00000676399.1:n.1921C>A
ENST00000676409.1:n.2078C>A
ENST00000300417.10:c.2018C>A	ENSP00000300417.6:p.Ser673Ter
ENST00000323301.8:c.2018C>A	ENSP00000322937.4:p.Ser673Ter
ENST00000373322.1:c.2018C>A	ENSP00000362419.1:p.Ser673Ter
ENST00000373324.8:c.1937C>A	ENSP00000362421.4:p.Ser646Ter
ENST00000483302.5:n.1240C>A
NM_001005373.3:c.2018C>A	NP_001005373.1:p.Ser673Ter
NM_001005374.3:c.2018C>A	NP_001005374.1:p.Ser673Ter
NM_001190723.2:c.1937C>A	NP_001177652.1:p.Ser646Ter
NM_138361.5:c.2018C>A , LRG_373t1:c.2018C>A	NP_612370.3:p.Ser673Ter
XM_006717316.2:c.1919C>A	XP_006717379.1:p.Ser640Ter
XM_006717316.4:c.1919C>A	XP_006717379.1:p.Ser640Ter
XM_017015283.1:c.2018C>A	XP_016870772.1:p.Ser673Ter
XM_017015284.2:c.1229C>A	XP_016870773.1:p.Ser410Ter
XR_001746415.2:n.2553C>A
XR_929874.3:n.2377C>A
NM_001190723.3:c.1937C>A	NP_001177652.1:p.Ser646Ter
NM_001005373.4:c.2018C>A MANE Select	NP_001005373.1:p.Ser673Ter
NM_001005374.4:c.2018C>A	NP_001005374.1:p.Ser673Ter
NM_001384142.1:c.2018C>A	NP_001371071.1:p.Ser673Ter
NM_001384143.1:c.1919C>A	NP_001371072.1:p.Ser640Ter
NM_001384144.1:c.1229C>A	NP_001371073.1:p.Ser410Ter
NR_168891.1:n.2547C>A
NR_168892.1:n.2371C>A