Canonical Allele Identifier: CA374938178

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263321C>G (hg19) ; chr9:g.127501042C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501042C>G , CM000671.2:g.127501042C>G	GRCh38
NC_000009.11:g.130263321C>G , CM000671.1:g.130263321C>G	GRCh37
NC_000009.10:g.129303142C>G	NCBI36
NG_032008.1:g.54557C>G , LRG_373:g.54557C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1945C>G MANE Select	ENSP00000300417.6:p.Pro649Ala
ENST00000472068.2:c.*1669C>G	ENSP00000501555.1:n.*1669C>G
ENST00000483302.6:n.2610C>G
ENST00000498513.6:c.*836C>G	ENSP00000501637.1:n.*836C>G
ENST00000674511.1:n.1544C>G
ENST00000674516.1:c.*561C>G	ENSP00000502441.1:n.*561C>G
ENST00000674621.1:n.1861-2331C>G
ENST00000674771.1:c.*588C>G	ENSP00000502627.1:n.*588C>G
ENST00000674784.1:c.*1005C>G	ENSP00000501837.1:n.*1005C>G
ENST00000674970.1:c.*1719C>G	ENSP00000502493.1:n.*1719C>G
ENST00000675012.1:n.1889C>G
ENST00000675141.1:c.1846C>G	ENSP00000502420.1:p.Pro616Ala
ENST00000675198.1:n.1825C>G
ENST00000675213.1:c.1900C>G	ENSP00000502218.1:p.Pro634Ala
ENST00000675224.1:c.*11C>G	ENSP00000501869.1:n.*11C>G
ENST00000675253.1:c.*617C>G	ENSP00000502557.1:n.*617C>G
ENST00000675445.1:c.*1617C>G	ENSP00000502253.1:n.*1617C>G
ENST00000675448.1:c.1945C>G	ENSP00000502167.1:p.Pro649Ala
ENST00000675521.1:n.1855C>G
ENST00000675572.1:c.1846C>G	ENSP00000501598.1:p.Pro616Ala
ENST00000675641.1:c.*687C>G	ENSP00000501845.1:n.*687C>G
ENST00000675657.1:c.*558C>G	ENSP00000502002.1:n.*558C>G
ENST00000675662.1:n.1740C>G
ENST00000675789.1:c.1765C>G	ENSP00000501954.1:p.Pro589Ala
ENST00000675883.1:c.1864C>G	ENSP00000501592.1:p.Pro622Ala
ENST00000675945.1:c.*586C>G	ENSP00000501835.1:n.*586C>G
ENST00000676014.1:c.1888C>G	ENSP00000502058.1:p.Pro630Ala
ENST00000676035.1:n.1607C>G
ENST00000676106.1:n.1982C>G
ENST00000676137.1:n.1975C>G
ENST00000676170.1:c.2026C>G	ENSP00000502177.1:p.Pro676Ala
ENST00000676318.1:c.*2775C>G	ENSP00000502300.1:n.*2775C>G
ENST00000676336.1:c.*558C>G	ENSP00000502686.1:n.*558C>G
ENST00000676349.1:c.*1633C>G	ENSP00000502155.1:n.*1633C>G
ENST00000676399.1:n.1848C>G
ENST00000676409.1:n.2005C>G
ENST00000300417.10:c.1945C>G	ENSP00000300417.6:p.Pro649Ala
ENST00000323301.8:c.1945C>G	ENSP00000322937.4:p.Pro649Ala
ENST00000373322.1:c.1945C>G	ENSP00000362419.1:p.Pro649Ala
ENST00000373324.8:c.1864C>G	ENSP00000362421.4:p.Pro622Ala
ENST00000472068.1:n.838C>G
ENST00000483302.5:n.1167C>G
NM_001005373.3:c.1945C>G	NP_001005373.1:p.Pro649Ala
NM_001005374.3:c.1945C>G	NP_001005374.1:p.Pro649Ala
NM_001190723.2:c.1864C>G	NP_001177652.1:p.Pro622Ala
NM_138361.5:c.1945C>G , LRG_373t1:c.1945C>G	NP_612370.3:p.Pro649Ala
XM_006717316.2:c.1846C>G	XP_006717379.1:p.Pro616Ala
XM_006717316.4:c.1846C>G	XP_006717379.1:p.Pro616Ala
XM_017015283.1:c.1945C>G	XP_016870772.1:p.Pro649Ala
XM_017015284.2:c.1156C>G	XP_016870773.1:p.Pro386Ala
XR_001746415.2:n.2480C>G
XR_929874.3:n.2304C>G
NM_001190723.3:c.1864C>G	NP_001177652.1:p.Pro622Ala
NM_001005373.4:c.1945C>G MANE Select	NP_001005373.1:p.Pro649Ala
NM_001005374.4:c.1945C>G	NP_001005374.1:p.Pro649Ala
NM_001384142.1:c.1945C>G	NP_001371071.1:p.Pro649Ala
NM_001384143.1:c.1846C>G	NP_001371072.1:p.Pro616Ala
NM_001384144.1:c.1156C>G	NP_001371073.1:p.Pro386Ala
NR_168891.1:n.2474C>G
NR_168892.1:n.2298C>G