Canonical Allele Identifier: CA2611691110

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533685_533692del , CM000673.2:g.533685_533692del GRCh38
NC_000011.9:g.533685_533692del , CM000673.1:g.533685_533692del GRCh37
NC_000011.8:g.523685_523692del NCBI36
NG_007666.1:g.6863_6870del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.291-76_291-69del (HRAS) ENSP00000380722.3:n.291-76_291-69del
ENST00000417302.7:c.291-76_291-69del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.291-76_291-69del
ENST00000397594.6:c.9-76_9-69del (HRAS) ENSP00000380722.2:n.9-76_9-69del
ENST00000417302.6:c.291-76_291-69del (HRAS) ENSP00000388246.1:n.291-76_291-69del
ENST00000462734.2:c.291-76_291-69del (HRAS) ENSP00000507303.1:n.291-76_291-69del
ENST00000311189.8:c.291-76_291-69del (HRAS) MANE Select ENSP00000309845.7:n.291-76_291-69del
ENST00000311189.7:c.291-76_291-69del (HRAS) ENSP00000309845.7:n.291-76_291-69del
ENST00000397594.5:c.291-76_291-69del (HRAS) ENSP00000380722.1:n.291-76_291-69del
ENST00000397596.6:c.291-76_291-69del (HRAS) ENSP00000380723.2:n.291-76_291-69del
ENST00000417302.5:c.291-76_291-69del (HRAS) ENSP00000388246.1:n.291-76_291-69del
ENST00000451590.5:c.291-76_291-69del (HRAS) ENSP00000407586.1:n.291-76_291-69del
ENST00000479482.1:n.212-76_212-69del (HRAS)
ENST00000493230.5:c.291-76_291-69del (HRAS) ENSP00000434023.1:n.291-76_291-69del
NM_001130442.1:c.291-76_291-69del (HRAS) NP_001123914.1:n.291-76_291-69del
NM_005343.2:c.291-76_291-69del (HRAS) NP_005334.1:n.291-76_291-69del
NM_176795.3:c.291-76_291-69del (HRAS) NP_789765.1:n.291-76_291-69del
XM_011519875.1:c.-424-4913_-424-4906del (LRRC56) XP_011518177.1:n.-424-4913_-424-4906del
XM_011519877.1:c.-162+5348_-162+5355del (LRRC56) XP_011518179.1:n.-162+5348_-162+5355del
XR_242795.1:n.490-76_490-69del (HRAS)
NM_001130442.2:c.291-76_291-69del (HRAS) NP_001123914.1:n.291-76_291-69del
NM_001318054.1:c.-29-76_-29-69del (HRAS) NP_001304983.1:n.-29-76_-29-69del
NM_005343.3:c.291-76_291-69del (HRAS) NP_005334.1:n.291-76_291-69del
NM_176795.4:c.291-76_291-69del (HRAS) NP_789765.1:n.291-76_291-69del
XM_011519875.2:c.-424-4913_-424-4906del (LRRC56) XP_011518177.1:n.-424-4913_-424-4906del
XM_011519877.2:c.-162+5348_-162+5355del (LRRC56) XP_011518179.1:n.-162+5348_-162+5355del
XM_017017167.1:c.-499-4838_-499-4831del (LRRC56) XP_016872656.1:n.-499-4838_-499-4831del
XM_017017168.1:c.-499-4838_-499-4831del (LRRC56) XP_016872657.1:n.-499-4838_-499-4831del
NM_005343.4:c.291-76_291-69del (HRAS) MANE Select NP_005334.1:n.291-76_291-69del
NM_001318054.2:c.-29-76_-29-69del (HRAS) NP_001304983.1:n.-29-76_-29-69del
NM_001130442.3:c.291-76_291-69del (HRAS) NP_001123914.1:n.291-76_291-69del
NM_176795.5:c.291-76_291-69del (HRAS) MANE Plus Clinical NP_789765.1:n.291-76_291-69del