Canonical Allele Identifier: CA467236658

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263323T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501044T>G , CM000671.2:g.127501044T>G	GRCh38
NC_000009.11:g.130263323T>G , CM000671.1:g.130263323T>G	GRCh37
NC_000009.10:g.129303144T>G	NCBI36
NG_032008.1:g.54559T>G , LRG_373:g.54559T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1947T>G MANE Select	ENSP00000300417.6:p.Pro649=
ENST00000472068.2:c.*1671T>G	ENSP00000501555.1:n.*1671T>G
ENST00000483302.6:n.2612T>G
ENST00000498513.6:c.*838T>G	ENSP00000501637.1:n.*838T>G
ENST00000674511.1:n.1546T>G
ENST00000674516.1:c.*563T>G	ENSP00000502441.1:n.*563T>G
ENST00000674621.1:n.1861-2329T>G
ENST00000674771.1:c.*590T>G	ENSP00000502627.1:n.*590T>G
ENST00000674784.1:c.*1007T>G	ENSP00000501837.1:n.*1007T>G
ENST00000674970.1:c.*1721T>G	ENSP00000502493.1:n.*1721T>G
ENST00000675012.1:n.1891T>G
ENST00000675141.1:c.1848T>G	ENSP00000502420.1:p.Pro616=
ENST00000675198.1:n.1827T>G
ENST00000675213.1:c.1902T>G	ENSP00000502218.1:p.Pro634=
ENST00000675224.1:c.*13T>G	ENSP00000501869.1:n.*13T>G
ENST00000675253.1:c.*619T>G	ENSP00000502557.1:n.*619T>G
ENST00000675445.1:c.*1619T>G	ENSP00000502253.1:n.*1619T>G
ENST00000675448.1:c.1947T>G	ENSP00000502167.1:p.Pro649=
ENST00000675521.1:n.1857T>G
ENST00000675572.1:c.1848T>G	ENSP00000501598.1:p.Pro616=
ENST00000675641.1:c.*689T>G	ENSP00000501845.1:n.*689T>G
ENST00000675657.1:c.*560T>G	ENSP00000502002.1:n.*560T>G
ENST00000675662.1:n.1742T>G
ENST00000675789.1:c.1767T>G	ENSP00000501954.1:p.Pro589=
ENST00000675883.1:c.1866T>G	ENSP00000501592.1:p.Pro622=
ENST00000675945.1:c.*588T>G	ENSP00000501835.1:n.*588T>G
ENST00000676014.1:c.1890T>G	ENSP00000502058.1:p.Pro630=
ENST00000676035.1:n.1609T>G
ENST00000676106.1:n.1984T>G
ENST00000676137.1:n.1977T>G
ENST00000676170.1:c.2028T>G	ENSP00000502177.1:p.Pro676=
ENST00000676318.1:c.*2777T>G	ENSP00000502300.1:n.*2777T>G
ENST00000676336.1:c.*560T>G	ENSP00000502686.1:n.*560T>G
ENST00000676349.1:c.*1635T>G	ENSP00000502155.1:n.*1635T>G
ENST00000676399.1:n.1850T>G
ENST00000676409.1:n.2007T>G
ENST00000300417.10:c.1947T>G	ENSP00000300417.6:p.Pro649=
ENST00000323301.8:c.1947T>G	ENSP00000322937.4:p.Pro649=
ENST00000373322.1:c.1947T>G	ENSP00000362419.1:p.Pro649=
ENST00000373324.8:c.1866T>G	ENSP00000362421.4:p.Pro622=
ENST00000472068.1:n.840T>G
ENST00000483302.5:n.1169T>G
NM_001005373.3:c.1947T>G	NP_001005373.1:p.Pro649=
NM_001005374.3:c.1947T>G	NP_001005374.1:p.Pro649=
NM_001190723.2:c.1866T>G	NP_001177652.1:p.Pro622=
NM_138361.5:c.1947T>G , LRG_373t1:c.1947T>G	NP_612370.3:p.Pro649=
XM_006717316.2:c.1848T>G	XP_006717379.1:p.Pro616=
XM_006717316.4:c.1848T>G	XP_006717379.1:p.Pro616=
XM_017015283.1:c.1947T>G	XP_016870772.1:p.Pro649=
XM_017015284.2:c.1158T>G	XP_016870773.1:p.Pro386=
XR_001746415.2:n.2482T>G
XR_929874.3:n.2306T>G
NM_001190723.3:c.1866T>G	NP_001177652.1:p.Pro622=
NM_001005373.4:c.1947T>G MANE Select	NP_001005373.1:p.Pro649=
NM_001005374.4:c.1947T>G	NP_001005374.1:p.Pro649=
NM_001384142.1:c.1947T>G	NP_001371071.1:p.Pro649=
NM_001384143.1:c.1848T>G	NP_001371072.1:p.Pro616=
NM_001384144.1:c.1158T>G	NP_001371073.1:p.Pro386=
NR_168891.1:n.2476T>G
NR_168892.1:n.2300T>G