Canonical Allele Identifier: CA374938174

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263319C>A (hg19) ; chr9:g.127501040C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501040C>A , CM000671.2:g.127501040C>A	GRCh38
NC_000009.11:g.130263319C>A , CM000671.1:g.130263319C>A	GRCh37
NC_000009.10:g.129303140C>A	NCBI36
NG_032008.1:g.54555C>A , LRG_373:g.54555C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1943C>A MANE Select	ENSP00000300417.6:p.Thr648Asn
ENST00000472068.2:c.*1667C>A	ENSP00000501555.1:n.*1667C>A
ENST00000483302.6:n.2608C>A
ENST00000498513.6:c.*834C>A	ENSP00000501637.1:n.*834C>A
ENST00000674511.1:n.1542C>A
ENST00000674516.1:c.*559C>A	ENSP00000502441.1:n.*559C>A
ENST00000674621.1:n.1861-2333C>A
ENST00000674771.1:c.*586C>A	ENSP00000502627.1:n.*586C>A
ENST00000674784.1:c.*1003C>A	ENSP00000501837.1:n.*1003C>A
ENST00000674970.1:c.*1717C>A	ENSP00000502493.1:n.*1717C>A
ENST00000675012.1:n.1887C>A
ENST00000675141.1:c.1844C>A	ENSP00000502420.1:p.Thr615Asn
ENST00000675198.1:n.1823C>A
ENST00000675213.1:c.1898C>A	ENSP00000502218.1:p.Thr633Asn
ENST00000675224.1:c.*9C>A	ENSP00000501869.1:n.*9C>A
ENST00000675253.1:c.*615C>A	ENSP00000502557.1:n.*615C>A
ENST00000675445.1:c.*1615C>A	ENSP00000502253.1:n.*1615C>A
ENST00000675448.1:c.1943C>A	ENSP00000502167.1:p.Thr648Asn
ENST00000675521.1:n.1853C>A
ENST00000675572.1:c.1844C>A	ENSP00000501598.1:p.Thr615Asn
ENST00000675641.1:c.*685C>A	ENSP00000501845.1:n.*685C>A
ENST00000675657.1:c.*556C>A	ENSP00000502002.1:n.*556C>A
ENST00000675662.1:n.1738C>A
ENST00000675789.1:c.1763C>A	ENSP00000501954.1:p.Thr588Asn
ENST00000675883.1:c.1862C>A	ENSP00000501592.1:p.Thr621Asn
ENST00000675945.1:c.*584C>A	ENSP00000501835.1:n.*584C>A
ENST00000676014.1:c.1886C>A	ENSP00000502058.1:p.Thr629Asn
ENST00000676035.1:n.1605C>A
ENST00000676106.1:n.1980C>A
ENST00000676137.1:n.1973C>A
ENST00000676170.1:c.2024C>A	ENSP00000502177.1:p.Thr675Asn
ENST00000676318.1:c.*2773C>A	ENSP00000502300.1:n.*2773C>A
ENST00000676336.1:c.*556C>A	ENSP00000502686.1:n.*556C>A
ENST00000676349.1:c.*1631C>A	ENSP00000502155.1:n.*1631C>A
ENST00000676399.1:n.1846C>A
ENST00000676409.1:n.2003C>A
ENST00000300417.10:c.1943C>A	ENSP00000300417.6:p.Thr648Asn
ENST00000323301.8:c.1943C>A	ENSP00000322937.4:p.Thr648Asn
ENST00000373322.1:c.1943C>A	ENSP00000362419.1:p.Thr648Asn
ENST00000373324.8:c.1862C>A	ENSP00000362421.4:p.Thr621Asn
ENST00000472068.1:n.836C>A
ENST00000483302.5:n.1165C>A
NM_001005373.3:c.1943C>A	NP_001005373.1:p.Thr648Asn
NM_001005374.3:c.1943C>A	NP_001005374.1:p.Thr648Asn
NM_001190723.2:c.1862C>A	NP_001177652.1:p.Thr621Asn
NM_138361.5:c.1943C>A , LRG_373t1:c.1943C>A	NP_612370.3:p.Thr648Asn
XM_006717316.2:c.1844C>A	XP_006717379.1:p.Thr615Asn
XM_006717316.4:c.1844C>A	XP_006717379.1:p.Thr615Asn
XM_017015283.1:c.1943C>A	XP_016870772.1:p.Thr648Asn
XM_017015284.2:c.1154C>A	XP_016870773.1:p.Thr385Asn
XR_001746415.2:n.2478C>A
XR_929874.3:n.2302C>A
NM_001190723.3:c.1862C>A	NP_001177652.1:p.Thr621Asn
NM_001005373.4:c.1943C>A MANE Select	NP_001005373.1:p.Thr648Asn
NM_001005374.4:c.1943C>A	NP_001005374.1:p.Thr648Asn
NM_001384142.1:c.1943C>A	NP_001371071.1:p.Thr648Asn
NM_001384143.1:c.1844C>A	NP_001371072.1:p.Thr615Asn
NM_001384144.1:c.1154C>A	NP_001371073.1:p.Thr385Asn
NR_168891.1:n.2472C>A
NR_168892.1:n.2296C>A