Canonical Allele Identifier: CA374932482

Gene: LRSAM1

Linked Data

• dbSNP Id: rs1835708694
• MyVariant Identifiers: chr9:g.130248086C>T (hg19) ; chr9:g.127485807C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127485807C>T , CM000671.2:g.127485807C>T	GRCh38
NC_000009.11:g.130248086C>T , CM000671.1:g.130248086C>T	GRCh37
NC_000009.10:g.129287907C>T	NCBI36
NG_032008.1:g.39322C>T , LRG_373:g.39322C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300417.11:c.1231C>T MANE Select	ENSP00000300417.6:p.Gln411Ter
ENST00000472068.2:c.*954C>T	ENSP00000501555.1:n.*954C>T
ENST00000498513.6:c.484C>T	ENSP00000501637.1:p.Gln162Ter
ENST00000674511.1:n.1106C>T
ENST00000674516.1:c.1231C>T	ENSP00000502441.1:p.Gln411Ter
ENST00000674621.1:n.1137C>T
ENST00000674771.1:c.1231C>T	ENSP00000502627.1:p.Gln411Ter
ENST00000674784.1:c.*390C>T	ENSP00000501837.1:n.*390C>T
ENST00000674970.1:c.*1005C>T	ENSP00000502493.1:n.*1005C>T
ENST00000675012.1:n.1111C>T
ENST00000675141.1:c.1231C>T	ENSP00000502420.1:p.Gln411Ter
ENST00000675198.1:n.1133C>T
ENST00000675213.1:c.1186C>T	ENSP00000502218.1:p.Gln396Ter
ENST00000675224.1:c.1231C>T	ENSP00000501869.1:p.Gln411Ter
ENST00000675253.1:c.1231C>T	ENSP00000502557.1:p.Gln411Ter
ENST00000675445.1:c.*903C>T	ENSP00000502253.1:n.*903C>T
ENST00000675448.1:c.1231C>T	ENSP00000502167.1:p.Gln411Ter
ENST00000675521.1:n.1083C>T
ENST00000675572.1:c.1231C>T	ENSP00000501598.1:p.Gln411Ter
ENST00000675641.1:c.1231C>T	ENSP00000501845.1:p.Gln411Ter
ENST00000675657.1:c.1231C>T	ENSP00000502002.1:p.Gln411Ter
ENST00000675662.1:n.1082+42C>T
ENST00000675789.1:c.1231C>T	ENSP00000501954.1:p.Gln411Ter
ENST00000675883.1:c.1231C>T	ENSP00000501592.1:p.Gln411Ter
ENST00000675945.1:c.1231C>T	ENSP00000501835.1:p.Gln411Ter
ENST00000676014.1:c.1174C>T	ENSP00000502058.1:p.Gln392Ter
ENST00000676035.1:n.992C>T
ENST00000676106.1:n.1036C>T
ENST00000676137.1:n.1122C>T
ENST00000676170.1:c.1312C>T	ENSP00000502177.1:p.Gln438Ter
ENST00000676318.1:c.1231C>T	ENSP00000502300.1:p.Gln411Ter
ENST00000676336.1:c.1009C>T	ENSP00000502686.1:p.Gln337Ter
ENST00000676349.1:c.*1000C>T	ENSP00000502155.1:n.*1000C>T
ENST00000676399.1:n.1129C>T
ENST00000676409.1:n.1110C>T
ENST00000300417.10:c.1231C>T	ENSP00000300417.6:p.Gln411Ter
ENST00000323301.8:c.1231C>T	ENSP00000322937.4:p.Gln411Ter
ENST00000373322.1:c.1231C>T	ENSP00000362419.1:p.Gln411Ter
ENST00000373324.8:c.1231C>T	ENSP00000362421.4:p.Gln411Ter
ENST00000472068.1:n.218C>T
ENST00000483302.5:n.448C>T
ENST00000498513.5:n.484C>T
NM_001005373.3:c.1231C>T	NP_001005373.1:p.Gln411Ter
NM_001005374.3:c.1231C>T	NP_001005374.1:p.Gln411Ter
NM_001190723.2:c.1231C>T	NP_001177652.1:p.Gln411Ter
NM_138361.5:c.1231C>T , LRG_373t1:c.1231C>T	NP_612370.3:p.Gln411Ter
XM_006717316.2:c.1231C>T	XP_006717379.1:p.Gln411Ter
XR_929874.1:n.1603C>T
XM_006717316.4:c.1231C>T	XP_006717379.1:p.Gln411Ter
XM_017015283.1:c.1231C>T	XP_016870772.1:p.Gln411Ter
XM_017015284.2:c.442C>T	XP_016870773.1:p.Gln148Ter
XR_001746415.2:n.1585C>T
XR_929874.3:n.1585C>T
NM_001190723.3:c.1231C>T	NP_001177652.1:p.Gln411Ter
NM_001005373.4:c.1231C>T MANE Select	NP_001005373.1:p.Gln411Ter
NM_001005374.4:c.1231C>T	NP_001005374.1:p.Gln411Ter
NM_001384142.1:c.1231C>T	NP_001371071.1:p.Gln411Ter
NM_001384143.1:c.1231C>T	NP_001371072.1:p.Gln411Ter
NM_001384144.1:c.442C>T	NP_001371073.1:p.Gln148Ter
NR_168891.1:n.1579C>T
NR_168892.1:n.1579C>T