Canonical Allele Identifier: CA374938300

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263385T>A (hg19) ; chr9:g.127501106T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501106T>A , CM000671.2:g.127501106T>A	GRCh38
NC_000009.11:g.130263385T>A , CM000671.1:g.130263385T>A	GRCh37
NC_000009.10:g.129303206T>A	NCBI36
NG_032008.1:g.54621T>A , LRG_373:g.54621T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2009T>A MANE Select	ENSP00000300417.6:p.Val670Glu
ENST00000472068.2:c.*1733T>A	ENSP00000501555.1:n.*1733T>A
ENST00000483302.6:n.2674T>A
ENST00000498513.6:c.*900T>A	ENSP00000501637.1:n.*900T>A
ENST00000674511.1:n.1608T>A
ENST00000674516.1:c.*625T>A	ENSP00000502441.1:n.*625T>A
ENST00000674621.1:n.1861-2267T>A
ENST00000674771.1:c.*652T>A	ENSP00000502627.1:n.*652T>A
ENST00000674784.1:c.*1069T>A	ENSP00000501837.1:n.*1069T>A
ENST00000674970.1:c.*1783T>A	ENSP00000502493.1:n.*1783T>A
ENST00000675012.1:n.1953T>A
ENST00000675141.1:c.1910T>A	ENSP00000502420.1:p.Val637Glu
ENST00000675198.1:n.1889T>A
ENST00000675213.1:c.1964T>A	ENSP00000502218.1:p.Val655Glu
ENST00000675224.1:c.*75T>A	ENSP00000501869.1:n.*75T>A
ENST00000675253.1:c.*681T>A	ENSP00000502557.1:n.*681T>A
ENST00000675445.1:c.*1681T>A	ENSP00000502253.1:n.*1681T>A
ENST00000675448.1:c.2009T>A	ENSP00000502167.1:p.Val670Glu
ENST00000675521.1:n.1919T>A
ENST00000675572.1:c.1910T>A	ENSP00000501598.1:p.Val637Glu
ENST00000675641.1:c.*751T>A	ENSP00000501845.1:n.*751T>A
ENST00000675657.1:c.*622T>A	ENSP00000502002.1:n.*622T>A
ENST00000675662.1:n.1804T>A
ENST00000675789.1:c.1829T>A	ENSP00000501954.1:p.Val610Glu
ENST00000675883.1:c.1928T>A	ENSP00000501592.1:p.Val643Glu
ENST00000675945.1:c.*650T>A	ENSP00000501835.1:n.*650T>A
ENST00000676014.1:c.1952T>A	ENSP00000502058.1:p.Val651Glu
ENST00000676035.1:n.1671T>A
ENST00000676106.1:n.2046T>A
ENST00000676137.1:n.2039T>A
ENST00000676170.1:c.2090T>A	ENSP00000502177.1:p.Val697Glu
ENST00000676318.1:c.*2839T>A	ENSP00000502300.1:n.*2839T>A
ENST00000676336.1:c.*622T>A	ENSP00000502686.1:n.*622T>A
ENST00000676349.1:c.*1697T>A	ENSP00000502155.1:n.*1697T>A
ENST00000676399.1:n.1912T>A
ENST00000676409.1:n.2069T>A
ENST00000300417.10:c.2009T>A	ENSP00000300417.6:p.Val670Glu
ENST00000323301.8:c.2009T>A	ENSP00000322937.4:p.Val670Glu
ENST00000373322.1:c.2009T>A	ENSP00000362419.1:p.Val670Glu
ENST00000373324.8:c.1928T>A	ENSP00000362421.4:p.Val643Glu
ENST00000483302.5:n.1231T>A
NM_001005373.3:c.2009T>A	NP_001005373.1:p.Val670Glu
NM_001005374.3:c.2009T>A	NP_001005374.1:p.Val670Glu
NM_001190723.2:c.1928T>A	NP_001177652.1:p.Val643Glu
NM_138361.5:c.2009T>A , LRG_373t1:c.2009T>A	NP_612370.3:p.Val670Glu
XM_006717316.2:c.1910T>A	XP_006717379.1:p.Val637Glu
XM_006717316.4:c.1910T>A	XP_006717379.1:p.Val637Glu
XM_017015283.1:c.2009T>A	XP_016870772.1:p.Val670Glu
XM_017015284.2:c.1220T>A	XP_016870773.1:p.Val407Glu
XR_001746415.2:n.2544T>A
XR_929874.3:n.2368T>A
NM_001190723.3:c.1928T>A	NP_001177652.1:p.Val643Glu
NM_001005373.4:c.2009T>A MANE Select	NP_001005373.1:p.Val670Glu
NM_001005374.4:c.2009T>A	NP_001005374.1:p.Val670Glu
NM_001384142.1:c.2009T>A	NP_001371071.1:p.Val670Glu
NM_001384143.1:c.1910T>A	NP_001371072.1:p.Val637Glu
NM_001384144.1:c.1220T>A	NP_001371073.1:p.Val407Glu
NR_168891.1:n.2538T>A
NR_168892.1:n.2362T>A