Canonical Allele Identifier: CA1879835744
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127485801C= , CM000671.2:g.127485801C= GRCh38
NC_000009.11:g.130248080C= , CM000671.1:g.130248080C= GRCh37
NC_000009.10:g.129287901C= NCBI36
NG_032008.1:g.39316C= , LRG_373:g.39316C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300417.11:c.1225C= MANE Select ENSP00000300417.6:p.Gln409=
ENST00000472068.2:c.*948C= ENSP00000501555.1:n.*948C=
ENST00000498513.6:c.478C= ENSP00000501637.1:p.Gln160=
ENST00000674511.1:n.1100C=
ENST00000674516.1:c.1225C= ENSP00000502441.1:p.Gln409=
ENST00000674621.1:n.1131C=
ENST00000674771.1:c.1225C= ENSP00000502627.1:p.Gln409=
ENST00000674784.1:c.*384C= ENSP00000501837.1:n.*384C=
ENST00000674970.1:c.*999C= ENSP00000502493.1:n.*999C=
ENST00000675012.1:n.1105C=
ENST00000675141.1:c.1225C= ENSP00000502420.1:p.Gln409=
ENST00000675198.1:n.1127C=
ENST00000675213.1:c.1180C= ENSP00000502218.1:p.Gln394=
ENST00000675224.1:c.1225C= ENSP00000501869.1:p.Gln409=
ENST00000675253.1:c.1225C= ENSP00000502557.1:p.Gln409=
ENST00000675445.1:c.*897C= ENSP00000502253.1:n.*897C=
ENST00000675448.1:c.1225C= ENSP00000502167.1:p.Gln409=
ENST00000675521.1:n.1077C=
ENST00000675572.1:c.1225C= ENSP00000501598.1:p.Gln409=
ENST00000675641.1:c.1225C= ENSP00000501845.1:p.Gln409=
ENST00000675657.1:c.1225C= ENSP00000502002.1:p.Gln409=
ENST00000675662.1:n.1082+36C=
ENST00000675789.1:c.1225C= ENSP00000501954.1:p.Gln409=
ENST00000675883.1:c.1225C= ENSP00000501592.1:p.Gln409=
ENST00000675945.1:c.1225C= ENSP00000501835.1:p.Gln409=
ENST00000676014.1:c.1168C= ENSP00000502058.1:p.Gln390=
ENST00000676035.1:n.986C=
ENST00000676106.1:n.1030C=
ENST00000676137.1:n.1116C=
ENST00000676170.1:c.1306C= ENSP00000502177.1:p.Gln436=
ENST00000676318.1:c.1225C= ENSP00000502300.1:p.Gln409=
ENST00000676336.1:c.1003C= ENSP00000502686.1:p.Gln335=
ENST00000676349.1:c.*994C= ENSP00000502155.1:n.*994C=
ENST00000676399.1:n.1123C=
ENST00000676409.1:n.1104C=
ENST00000300417.10:c.1225C= ENSP00000300417.6:p.Gln409=
ENST00000323301.8:c.1225C= ENSP00000322937.4:p.Gln409=
ENST00000373322.1:c.1225C= ENSP00000362419.1:p.Gln409=
ENST00000373324.8:c.1225C= ENSP00000362421.4:p.Gln409=
ENST00000472068.1:n.212C=
ENST00000483302.5:n.442C=
ENST00000498513.5:n.478C=
NM_001005373.3:c.1225C= NP_001005373.1:p.Gln409=
NM_001005374.3:c.1225C= NP_001005374.1:p.Gln409=
NM_001190723.2:c.1225C= NP_001177652.1:p.Gln409=
NM_138361.5:c.1225C= , LRG_373t1:c.1225C= NP_612370.3:p.Gln409=
XM_006717316.2:c.1225C= XP_006717379.1:p.Gln409=
XR_929874.1:n.1597C=
XM_006717316.4:c.1225C= XP_006717379.1:p.Gln409=
XM_017015283.1:c.1225C= XP_016870772.1:p.Gln409=
XM_017015284.2:c.436C= XP_016870773.1:p.Gln146=
XR_001746415.2:n.1579C=
XR_929874.3:n.1579C=
NM_001190723.3:c.1225C= NP_001177652.1:p.Gln409=
NM_001005373.4:c.1225C= MANE Select NP_001005373.1:p.Gln409=
NM_001005374.4:c.1225C= NP_001005374.1:p.Gln409=
NM_001384142.1:c.1225C= NP_001371071.1:p.Gln409=
NM_001384143.1:c.1225C= NP_001371072.1:p.Gln409=
NM_001384144.1:c.436C= NP_001371073.1:p.Gln146=
NR_168891.1:n.1573C=
NR_168892.1:n.1573C=