Canonical Allele Identifier: CA467236921

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263392C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501113C>T , CM000671.2:g.127501113C>T	GRCh38
NC_000009.11:g.130263392C>T , CM000671.1:g.130263392C>T	GRCh37
NC_000009.10:g.129303213C>T	NCBI36
NG_032008.1:g.54628C>T , LRG_373:g.54628C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2016C>T MANE Select	ENSP00000300417.6:p.Ala672=
ENST00000472068.2:c.*1740C>T	ENSP00000501555.1:n.*1740C>T
ENST00000483302.6:n.2681C>T
ENST00000498513.6:c.*907C>T	ENSP00000501637.1:n.*907C>T
ENST00000674511.1:n.1615C>T
ENST00000674516.1:c.*632C>T	ENSP00000502441.1:n.*632C>T
ENST00000674621.1:n.1861-2260C>T
ENST00000674771.1:c.*659C>T	ENSP00000502627.1:n.*659C>T
ENST00000674784.1:c.*1076C>T	ENSP00000501837.1:n.*1076C>T
ENST00000674970.1:c.*1790C>T	ENSP00000502493.1:n.*1790C>T
ENST00000675012.1:n.1960C>T
ENST00000675141.1:c.1917C>T	ENSP00000502420.1:p.Ala639=
ENST00000675198.1:n.1896C>T
ENST00000675213.1:c.1971C>T	ENSP00000502218.1:p.Ala657=
ENST00000675224.1:c.*82C>T	ENSP00000501869.1:n.*82C>T
ENST00000675253.1:c.*688C>T	ENSP00000502557.1:n.*688C>T
ENST00000675445.1:c.*1688C>T	ENSP00000502253.1:n.*1688C>T
ENST00000675448.1:c.2016C>T	ENSP00000502167.1:p.Ala672=
ENST00000675521.1:n.1926C>T
ENST00000675572.1:c.1917C>T	ENSP00000501598.1:p.Ala639=
ENST00000675641.1:c.*758C>T	ENSP00000501845.1:n.*758C>T
ENST00000675657.1:c.*629C>T	ENSP00000502002.1:n.*629C>T
ENST00000675662.1:n.1811C>T
ENST00000675789.1:c.1836C>T	ENSP00000501954.1:p.Ala612=
ENST00000675883.1:c.1935C>T	ENSP00000501592.1:p.Ala645=
ENST00000675945.1:c.*657C>T	ENSP00000501835.1:n.*657C>T
ENST00000676014.1:c.1959C>T	ENSP00000502058.1:p.Ala653=
ENST00000676035.1:n.1678C>T
ENST00000676106.1:n.2053C>T
ENST00000676137.1:n.2046C>T
ENST00000676170.1:c.2097C>T	ENSP00000502177.1:p.Ala699=
ENST00000676318.1:c.*2846C>T	ENSP00000502300.1:n.*2846C>T
ENST00000676336.1:c.*629C>T	ENSP00000502686.1:n.*629C>T
ENST00000676349.1:c.*1704C>T	ENSP00000502155.1:n.*1704C>T
ENST00000676399.1:n.1919C>T
ENST00000676409.1:n.2076C>T
ENST00000300417.10:c.2016C>T	ENSP00000300417.6:p.Ala672=
ENST00000323301.8:c.2016C>T	ENSP00000322937.4:p.Ala672=
ENST00000373322.1:c.2016C>T	ENSP00000362419.1:p.Ala672=
ENST00000373324.8:c.1935C>T	ENSP00000362421.4:p.Ala645=
ENST00000483302.5:n.1238C>T
NM_001005373.3:c.2016C>T	NP_001005373.1:p.Ala672=
NM_001005374.3:c.2016C>T	NP_001005374.1:p.Ala672=
NM_001190723.2:c.1935C>T	NP_001177652.1:p.Ala645=
NM_138361.5:c.2016C>T , LRG_373t1:c.2016C>T	NP_612370.3:p.Ala672=
XM_006717316.2:c.1917C>T	XP_006717379.1:p.Ala639=
XM_006717316.4:c.1917C>T	XP_006717379.1:p.Ala639=
XM_017015283.1:c.2016C>T	XP_016870772.1:p.Ala672=
XM_017015284.2:c.1227C>T	XP_016870773.1:p.Ala409=
XR_001746415.2:n.2551C>T
XR_929874.3:n.2375C>T
NM_001190723.3:c.1935C>T	NP_001177652.1:p.Ala645=
NM_001005373.4:c.2016C>T MANE Select	NP_001005373.1:p.Ala672=
NM_001005374.4:c.2016C>T	NP_001005374.1:p.Ala672=
NM_001384142.1:c.2016C>T	NP_001371071.1:p.Ala672=
NM_001384143.1:c.1917C>T	NP_001371072.1:p.Ala639=
NM_001384144.1:c.1227C>T	NP_001371073.1:p.Ala409=
NR_168891.1:n.2545C>T
NR_168892.1:n.2369C>T