Canonical Allele Identifier: CA374938120

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263291C>A (hg19) ; chr9:g.127501012C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501012C>A , CM000671.2:g.127501012C>A	GRCh38
NC_000009.11:g.130263291C>A , CM000671.1:g.130263291C>A	GRCh37
NC_000009.10:g.129303112C>A	NCBI36
NG_032008.1:g.54527C>A , LRG_373:g.54527C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1915C>A MANE Select	ENSP00000300417.6:p.Leu639Met
ENST00000472068.2:c.*1639C>A	ENSP00000501555.1:n.*1639C>A
ENST00000483302.6:n.2580C>A
ENST00000498513.6:c.*806C>A	ENSP00000501637.1:n.*806C>A
ENST00000674511.1:n.1514C>A
ENST00000674516.1:c.*531C>A	ENSP00000502441.1:n.*531C>A
ENST00000674621.1:n.1861-2361C>A
ENST00000674771.1:c.*558C>A	ENSP00000502627.1:n.*558C>A
ENST00000674784.1:c.*975C>A	ENSP00000501837.1:n.*975C>A
ENST00000674970.1:c.*1689C>A	ENSP00000502493.1:n.*1689C>A
ENST00000675012.1:n.1859C>A
ENST00000675141.1:c.1816C>A	ENSP00000502420.1:p.Leu606Met
ENST00000675198.1:n.1795C>A
ENST00000675213.1:c.1870C>A	ENSP00000502218.1:p.Leu624Met
ENST00000675224.1:c.1943C>A	ENSP00000501869.1:p.Ala648Asp
ENST00000675253.1:c.*587C>A	ENSP00000502557.1:n.*587C>A
ENST00000675445.1:c.*1587C>A	ENSP00000502253.1:n.*1587C>A
ENST00000675448.1:c.1915C>A	ENSP00000502167.1:p.Leu639Met
ENST00000675521.1:n.1825C>A
ENST00000675572.1:c.1816C>A	ENSP00000501598.1:p.Leu606Met
ENST00000675641.1:c.*657C>A	ENSP00000501845.1:n.*657C>A
ENST00000675657.1:c.*528C>A	ENSP00000502002.1:n.*528C>A
ENST00000675662.1:n.1710C>A
ENST00000675789.1:c.1735C>A	ENSP00000501954.1:p.Leu579Met
ENST00000675883.1:c.1834C>A	ENSP00000501592.1:p.Leu612Met
ENST00000675945.1:c.*556C>A	ENSP00000501835.1:n.*556C>A
ENST00000676014.1:c.1858C>A	ENSP00000502058.1:p.Leu620Met
ENST00000676035.1:n.1577C>A
ENST00000676106.1:n.1952C>A
ENST00000676137.1:n.1945C>A
ENST00000676170.1:c.1996C>A	ENSP00000502177.1:p.Leu666Met
ENST00000676318.1:c.*2745C>A	ENSP00000502300.1:n.*2745C>A
ENST00000676336.1:c.*528C>A	ENSP00000502686.1:n.*528C>A
ENST00000676349.1:c.*1603C>A	ENSP00000502155.1:n.*1603C>A
ENST00000676399.1:n.1818C>A
ENST00000676409.1:n.1975C>A
ENST00000300417.10:c.1915C>A	ENSP00000300417.6:p.Leu639Met
ENST00000323301.8:c.1915C>A	ENSP00000322937.4:p.Leu639Met
ENST00000373322.1:c.1915C>A	ENSP00000362419.1:p.Leu639Met
ENST00000373324.8:c.1834C>A	ENSP00000362421.4:p.Leu612Met
ENST00000472068.1:n.808C>A
ENST00000483302.5:n.1137C>A
NM_001005373.3:c.1915C>A	NP_001005373.1:p.Leu639Met
NM_001005374.3:c.1915C>A	NP_001005374.1:p.Leu639Met
NM_001190723.2:c.1834C>A	NP_001177652.1:p.Leu612Met
NM_138361.5:c.1915C>A , LRG_373t1:c.1915C>A	NP_612370.3:p.Leu639Met
XM_006717316.2:c.1816C>A	XP_006717379.1:p.Leu606Met
XM_006717316.4:c.1816C>A	XP_006717379.1:p.Leu606Met
XM_017015283.1:c.1915C>A	XP_016870772.1:p.Leu639Met
XM_017015284.2:c.1126C>A	XP_016870773.1:p.Leu376Met
XR_001746415.2:n.2450C>A
XR_929874.3:n.2274C>A
NM_001190723.3:c.1834C>A	NP_001177652.1:p.Leu612Met
NM_001005373.4:c.1915C>A MANE Select	NP_001005373.1:p.Leu639Met
NM_001005374.4:c.1915C>A	NP_001005374.1:p.Leu639Met
NM_001384142.1:c.1915C>A	NP_001371071.1:p.Leu639Met
NM_001384143.1:c.1816C>A	NP_001371072.1:p.Leu606Met
NM_001384144.1:c.1126C>A	NP_001371073.1:p.Leu376Met
NR_168891.1:n.2444C>A
NR_168892.1:n.2268C>A