Canonical Allele Identifier: CA467236793

Gene: LRSAM1

Linked Data

• dbSNP Id: rs1836370823
• MyVariant Identifiers: chr9:g.130263359A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501080A>G , CM000671.2:g.127501080A>G	GRCh38
NC_000009.11:g.130263359A>G , CM000671.1:g.130263359A>G	GRCh37
NC_000009.10:g.129303180A>G	NCBI36
NG_032008.1:g.54595A>G , LRG_373:g.54595A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1983A>G MANE Select	ENSP00000300417.6:p.Pro661=
ENST00000472068.2:c.*1707A>G	ENSP00000501555.1:n.*1707A>G
ENST00000483302.6:n.2648A>G
ENST00000498513.6:c.*874A>G	ENSP00000501637.1:n.*874A>G
ENST00000674511.1:n.1582A>G
ENST00000674516.1:c.*599A>G	ENSP00000502441.1:n.*599A>G
ENST00000674621.1:n.1861-2293A>G
ENST00000674771.1:c.*626A>G	ENSP00000502627.1:n.*626A>G
ENST00000674784.1:c.*1043A>G	ENSP00000501837.1:n.*1043A>G
ENST00000674970.1:c.*1757A>G	ENSP00000502493.1:n.*1757A>G
ENST00000675012.1:n.1927A>G
ENST00000675141.1:c.1884A>G	ENSP00000502420.1:p.Pro628=
ENST00000675198.1:n.1863A>G
ENST00000675213.1:c.1938A>G	ENSP00000502218.1:p.Pro646=
ENST00000675224.1:c.*49A>G	ENSP00000501869.1:n.*49A>G
ENST00000675253.1:c.*655A>G	ENSP00000502557.1:n.*655A>G
ENST00000675445.1:c.*1655A>G	ENSP00000502253.1:n.*1655A>G
ENST00000675448.1:c.1983A>G	ENSP00000502167.1:p.Pro661=
ENST00000675521.1:n.1893A>G
ENST00000675572.1:c.1884A>G	ENSP00000501598.1:p.Pro628=
ENST00000675641.1:c.*725A>G	ENSP00000501845.1:n.*725A>G
ENST00000675657.1:c.*596A>G	ENSP00000502002.1:n.*596A>G
ENST00000675662.1:n.1778A>G
ENST00000675789.1:c.1803A>G	ENSP00000501954.1:p.Pro601=
ENST00000675883.1:c.1902A>G	ENSP00000501592.1:p.Pro634=
ENST00000675945.1:c.*624A>G	ENSP00000501835.1:n.*624A>G
ENST00000676014.1:c.1926A>G	ENSP00000502058.1:p.Pro642=
ENST00000676035.1:n.1645A>G
ENST00000676106.1:n.2020A>G
ENST00000676137.1:n.2013A>G
ENST00000676170.1:c.2064A>G	ENSP00000502177.1:p.Pro688=
ENST00000676318.1:c.*2813A>G	ENSP00000502300.1:n.*2813A>G
ENST00000676336.1:c.*596A>G	ENSP00000502686.1:n.*596A>G
ENST00000676349.1:c.*1671A>G	ENSP00000502155.1:n.*1671A>G
ENST00000676399.1:n.1886A>G
ENST00000676409.1:n.2043A>G
ENST00000300417.10:c.1983A>G	ENSP00000300417.6:p.Pro661=
ENST00000323301.8:c.1983A>G	ENSP00000322937.4:p.Pro661=
ENST00000373322.1:c.1983A>G	ENSP00000362419.1:p.Pro661=
ENST00000373324.8:c.1902A>G	ENSP00000362421.4:p.Pro634=
ENST00000483302.5:n.1205A>G
NM_001005373.3:c.1983A>G	NP_001005373.1:p.Pro661=
NM_001005374.3:c.1983A>G	NP_001005374.1:p.Pro661=
NM_001190723.2:c.1902A>G	NP_001177652.1:p.Pro634=
NM_138361.5:c.1983A>G , LRG_373t1:c.1983A>G	NP_612370.3:p.Pro661=
XM_006717316.2:c.1884A>G	XP_006717379.1:p.Pro628=
XM_006717316.4:c.1884A>G	XP_006717379.1:p.Pro628=
XM_017015283.1:c.1983A>G	XP_016870772.1:p.Pro661=
XM_017015284.2:c.1194A>G	XP_016870773.1:p.Pro398=
XR_001746415.2:n.2518A>G
XR_929874.3:n.2342A>G
NM_001190723.3:c.1902A>G	NP_001177652.1:p.Pro634=
NM_001005373.4:c.1983A>G MANE Select	NP_001005373.1:p.Pro661=
NM_001005374.4:c.1983A>G	NP_001005374.1:p.Pro661=
NM_001384142.1:c.1983A>G	NP_001371071.1:p.Pro661=
NM_001384143.1:c.1884A>G	NP_001371072.1:p.Pro628=
NM_001384144.1:c.1194A>G	NP_001371073.1:p.Pro398=
NR_168891.1:n.2512A>G
NR_168892.1:n.2336A>G