Canonical Allele Identifier: CA374938163

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263313T>A (hg19) ; chr9:g.127501034T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501034T>A , CM000671.2:g.127501034T>A	GRCh38
NC_000009.11:g.130263313T>A , CM000671.1:g.130263313T>A	GRCh37
NC_000009.10:g.129303134T>A	NCBI36
NG_032008.1:g.54549T>A , LRG_373:g.54549T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1937T>A MANE Select	ENSP00000300417.6:p.Val646Asp
ENST00000472068.2:c.*1661T>A	ENSP00000501555.1:n.*1661T>A
ENST00000483302.6:n.2602T>A
ENST00000498513.6:c.*828T>A	ENSP00000501637.1:n.*828T>A
ENST00000674511.1:n.1536T>A
ENST00000674516.1:c.*553T>A	ENSP00000502441.1:n.*553T>A
ENST00000674621.1:n.1861-2339T>A
ENST00000674771.1:c.*580T>A	ENSP00000502627.1:n.*580T>A
ENST00000674784.1:c.*997T>A	ENSP00000501837.1:n.*997T>A
ENST00000674970.1:c.*1711T>A	ENSP00000502493.1:n.*1711T>A
ENST00000675012.1:n.1881T>A
ENST00000675141.1:c.1838T>A	ENSP00000502420.1:p.Val613Asp
ENST00000675198.1:n.1817T>A
ENST00000675213.1:c.1892T>A	ENSP00000502218.1:p.Val631Asp
ENST00000675224.1:c.*3T>A	ENSP00000501869.1:n.*3T>A
ENST00000675253.1:c.*609T>A	ENSP00000502557.1:n.*609T>A
ENST00000675445.1:c.*1609T>A	ENSP00000502253.1:n.*1609T>A
ENST00000675448.1:c.1937T>A	ENSP00000502167.1:p.Val646Asp
ENST00000675521.1:n.1847T>A
ENST00000675572.1:c.1838T>A	ENSP00000501598.1:p.Val613Asp
ENST00000675641.1:c.*679T>A	ENSP00000501845.1:n.*679T>A
ENST00000675657.1:c.*550T>A	ENSP00000502002.1:n.*550T>A
ENST00000675662.1:n.1732T>A
ENST00000675789.1:c.1757T>A	ENSP00000501954.1:p.Val586Asp
ENST00000675883.1:c.1856T>A	ENSP00000501592.1:p.Val619Asp
ENST00000675945.1:c.*578T>A	ENSP00000501835.1:n.*578T>A
ENST00000676014.1:c.1880T>A	ENSP00000502058.1:p.Val627Asp
ENST00000676035.1:n.1599T>A
ENST00000676106.1:n.1974T>A
ENST00000676137.1:n.1967T>A
ENST00000676170.1:c.2018T>A	ENSP00000502177.1:p.Val673Asp
ENST00000676318.1:c.*2767T>A	ENSP00000502300.1:n.*2767T>A
ENST00000676336.1:c.*550T>A	ENSP00000502686.1:n.*550T>A
ENST00000676349.1:c.*1625T>A	ENSP00000502155.1:n.*1625T>A
ENST00000676399.1:n.1840T>A
ENST00000676409.1:n.1997T>A
ENST00000300417.10:c.1937T>A	ENSP00000300417.6:p.Val646Asp
ENST00000323301.8:c.1937T>A	ENSP00000322937.4:p.Val646Asp
ENST00000373322.1:c.1937T>A	ENSP00000362419.1:p.Val646Asp
ENST00000373324.8:c.1856T>A	ENSP00000362421.4:p.Val619Asp
ENST00000472068.1:n.830T>A
ENST00000483302.5:n.1159T>A
NM_001005373.3:c.1937T>A	NP_001005373.1:p.Val646Asp
NM_001005374.3:c.1937T>A	NP_001005374.1:p.Val646Asp
NM_001190723.2:c.1856T>A	NP_001177652.1:p.Val619Asp
NM_138361.5:c.1937T>A , LRG_373t1:c.1937T>A	NP_612370.3:p.Val646Asp
XM_006717316.2:c.1838T>A	XP_006717379.1:p.Val613Asp
XM_006717316.4:c.1838T>A	XP_006717379.1:p.Val613Asp
XM_017015283.1:c.1937T>A	XP_016870772.1:p.Val646Asp
XM_017015284.2:c.1148T>A	XP_016870773.1:p.Val383Asp
XR_001746415.2:n.2472T>A
XR_929874.3:n.2296T>A
NM_001190723.3:c.1856T>A	NP_001177652.1:p.Val619Asp
NM_001005373.4:c.1937T>A MANE Select	NP_001005373.1:p.Val646Asp
NM_001005374.4:c.1937T>A	NP_001005374.1:p.Val646Asp
NM_001384142.1:c.1937T>A	NP_001371071.1:p.Val646Asp
NM_001384143.1:c.1838T>A	NP_001371072.1:p.Val613Asp
NM_001384144.1:c.1148T>A	NP_001371073.1:p.Val383Asp
NR_168891.1:n.2466T>A
NR_168892.1:n.2290T>A