Canonical Allele Identifier: CA2723270591
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

dbSNP Id: rs2133990711
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533850_533855del , CM000673.2:g.533850_533855del GRCh38
NC_000011.9:g.533850_533855del , CM000673.1:g.533850_533855del GRCh37
NC_000011.8:g.523850_523855del NCBI36
NG_007666.1:g.6696_6701del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.201_206del (HRAS) ENSP00000380722.3:p.Met67_Asp69delinsIle
ENST00000417302.7:c.201_206del (HRAS) MANE Plus Clinical ENSP00000388246.1:p.Met67_Asp69delinsIle
ENST00000417302.6:c.201_206del (HRAS) ENSP00000388246.1:p.Met67_Asp69delinsIle
ENST00000462734.2:c.201_206del (HRAS) ENSP00000507303.1:p.Met67_Asp69delinsIle
ENST00000311189.8:c.201_206del (HRAS) MANE Select ENSP00000309845.7:p.Met67_Asp69delinsIle
ENST00000311189.7:c.201_206del (HRAS) ENSP00000309845.7:p.Met67_Asp69delinsIle
ENST00000397594.5:c.201_206del (HRAS) ENSP00000380722.1:p.Met67_Asp69delinsIle
ENST00000397596.6:c.201_206del (HRAS) ENSP00000380723.2:p.Met67_Asp69delinsIle
ENST00000417302.5:c.201_206del (HRAS) ENSP00000388246.1:p.Met67_Asp69delinsIle
ENST00000451590.5:c.201_206del (HRAS) ENSP00000407586.1:p.Met67_Asp69delinsIle
ENST00000468682.2:n.689_694del (HRAS)
ENST00000479482.1:n.122_127del (HRAS)
ENST00000493230.5:c.201_206del (HRAS) ENSP00000434023.1:p.Met67_Asp69delinsIle
NM_001130442.1:c.201_206del (HRAS) NP_001123914.1:p.Met67_Asp69delinsIle
NM_005343.2:c.201_206del (HRAS) NP_005334.1:p.Met67_Asp69delinsIle
NM_176795.3:c.201_206del (HRAS) NP_789765.1:p.Met67_Asp69delinsIle
XM_011519875.1:c.-424-4748_-424-4743del (LRRC56) XP_011518177.1:n.-424-4748_-424-4743del
XM_011519877.1:c.-162+5513_-162+5518del (LRRC56) XP_011518179.1:n.-162+5513_-162+5518del
XR_242795.1:n.400_405del (HRAS)
NM_001130442.2:c.201_206del (HRAS) NP_001123914.1:p.Met67_Asp69delinsIle
NM_001318054.1:c.-119_-114del (HRAS) NP_001304983.1:n.-119_-114del
NM_005343.3:c.201_206del (HRAS) NP_005334.1:p.Met67_Asp69delinsIle
NM_176795.4:c.201_206del (HRAS) NP_789765.1:p.Met67_Asp69delinsIle
XM_011519875.2:c.-424-4748_-424-4743del (LRRC56) XP_011518177.1:n.-424-4748_-424-4743del
XM_011519877.2:c.-162+5513_-162+5518del (LRRC56) XP_011518179.1:n.-162+5513_-162+5518del
XM_017017167.1:c.-499-4673_-499-4668del (LRRC56) XP_016872656.1:n.-499-4673_-499-4668del
XM_017017168.1:c.-499-4673_-499-4668del (LRRC56) XP_016872657.1:n.-499-4673_-499-4668del
NM_005343.4:c.201_206del (HRAS) MANE Select NP_005334.1:p.Met67_Asp69delinsIle
NM_001318054.2:c.-119_-114del (HRAS) NP_001304983.1:n.-119_-114del
NM_001130442.3:c.201_206del (HRAS) NP_001123914.1:p.Met67_Asp69delinsIle
NM_176795.5:c.201_206del (HRAS) MANE Plus Clinical NP_789765.1:p.Met67_Asp69delinsIle
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