Canonical Allele Identifier: CA374935237
Community Standard Title: NM_001005373.4(LRSAM1):c.1641C>G (p.Tyr547Ter)
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127495361C>G , CM000671.2:g.127495361C>G GRCh38
NC_000009.11:g.130257640C>G , CM000671.1:g.130257640C>G GRCh37
NC_000009.10:g.129297461C>G NCBI36
NG_032008.1:g.48876C>G , LRG_373:g.48876C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001005373.4:c.1641C>G MANE Select NP_001005373.1:p.Tyr547Ter
ENST00000300417.11:c.1641C>G MANE Select ENSP00000300417.6:p.Tyr547Ter
NM_001005373.3:c.1641C>G NP_001005373.1:p.Tyr547Ter
NM_001005374.3:c.1641C>G NP_001005374.1:p.Tyr547Ter
NM_001005374.4:c.1641C>G NP_001005374.1:p.Tyr547Ter
NM_001190723.2:c.1560C>G NP_001177652.1:p.Tyr520Ter
NM_001190723.3:c.1560C>G NP_001177652.1:p.Tyr520Ter
NM_001384142.1:c.1641C>G NP_001371071.1:p.Tyr547Ter
NM_001384143.1:c.1600-603C>G NP_001371072.1:n.1600-603C>G
NM_001384144.1:c.852C>G NP_001371073.1:p.Tyr284Ter
NM_138361.5:c.1641C>G , LRG_373t1:c.1641C>G NP_612370.3:p.Tyr547Ter
NR_168891.1:n.2170C>G
NR_168892.1:n.1994C>G
ENST00000300417.10:c.1641C>G ENSP00000300417.6:p.Tyr547Ter
ENST00000323301.8:c.1641C>G ENSP00000322937.4:p.Tyr547Ter
ENST00000373322.1:c.1641C>G ENSP00000362419.1:p.Tyr547Ter
ENST00000373324.8:c.1560C>G ENSP00000362421.4:p.Tyr520Ter
ENST00000472068.1:n.592-603C>G
ENST00000472068.2:c.*1369C>G ENSP00000501555.1:n.*1369C>G
ENST00000483302.5:n.863C>G
ENST00000483302.6:n.2306C>G
ENST00000498513.6:c.*532C>G ENSP00000501637.1:n.*532C>G
ENST00000674511.1:n.1298-603C>G
ENST00000674516.1:c.1641C>G ENSP00000502441.1:p.Tyr547Ter
ENST00000674621.1:n.1691C>G
ENST00000674771.1:c.*342-603C>G ENSP00000502627.1:n.*342-603C>G
ENST00000674784.1:c.*759-603C>G ENSP00000501837.1:n.*759-603C>G
ENST00000674970.1:c.*1415C>G ENSP00000502493.1:n.*1415C>G
ENST00000675012.1:n.1585C>G
ENST00000675141.1:c.1600-603C>G ENSP00000502420.1:n.1600-603C>G
ENST00000675198.1:n.1521C>G
ENST00000675213.1:c.1596C>G ENSP00000502218.1:p.Tyr532Ter
ENST00000675224.1:c.1641C>G ENSP00000501869.1:p.Tyr547Ter
ENST00000675253.1:c.*371-603C>G ENSP00000502557.1:n.*371-603C>G
ENST00000675445.1:c.*1313C>G ENSP00000502253.1:n.*1313C>G
ENST00000675448.1:c.1641C>G ENSP00000502167.1:p.Tyr547Ter
ENST00000675521.1:n.1551C>G
ENST00000675572.1:c.1600-603C>G ENSP00000501598.1:n.1600-603C>G
ENST00000675641.1:c.*383C>G ENSP00000501845.1:n.*383C>G
ENST00000675657.1:c.*254C>G ENSP00000502002.1:n.*254C>G
ENST00000675662.1:n.1436C>G
ENST00000675789.1:c.1519-603C>G ENSP00000501954.1:n.1519-603C>G
ENST00000675883.1:c.1560C>G ENSP00000501592.1:p.Tyr520Ter
ENST00000675945.1:c.*422-603C>G ENSP00000501835.1:n.*422-603C>G
ENST00000676014.1:c.1584C>G ENSP00000502058.1:p.Tyr528Ter
ENST00000676035.1:n.1361-603C>G
ENST00000676106.1:n.1736-603C>G
ENST00000676137.1:n.1671C>G
ENST00000676170.1:c.1722C>G ENSP00000502177.1:p.Tyr574Ter
ENST00000676318.1:c.*2471C>G ENSP00000502300.1:n.*2471C>G
ENST00000676336.1:c.*254C>G ENSP00000502686.1:n.*254C>G
ENST00000676349.1:c.*1329C>G ENSP00000502155.1:n.*1329C>G
ENST00000676399.1:n.1544C>G
ENST00000676409.1:n.1701C>G
XM_006717316.2:c.1600-603C>G XP_006717379.1:n.1600-603C>G
XM_006717316.4:c.1600-603C>G XP_006717379.1:n.1600-603C>G
XM_017015283.1:c.1641C>G XP_016870772.1:p.Tyr547Ter
XM_017015284.2:c.852C>G XP_016870773.1:p.Tyr284Ter
XR_001746415.2:n.2176C>G
XR_929874.3:n.2000C>G