Canonical Allele Identifier: CA2611691564
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

gnomAD v4: 11-532466-CCTCCTTCCGTCTGCACCTCCTTCCTG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532468_532493del , CM000673.2:g.532468_532493del GRCh38
NC_000011.9:g.532468_532493del , CM000673.1:g.532468_532493del GRCh37
NC_000011.8:g.522468_522493del NCBI36
NG_007666.1:g.8059_8084del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*158_*183del (HRAS) ENSP00000380722.3:n.*158_*183del
ENST00000417302.7:c.*283_*308del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*283_*308del
ENST00000397594.6:c.389_414del (HRAS) ENSP00000380722.2:n.389_414del
ENST00000417302.6:c.*283_*308del (HRAS) ENSP00000388246.1:n.*283_*308del
ENST00000462734.2:c.*218_*243del (HRAS) ENSP00000507303.1:n.*218_*243del
ENST00000311189.8:c.*36_*61del (HRAS) MANE Select ENSP00000309845.7:n.*36_*61del
ENST00000311189.7:c.*36_*61del (HRAS) ENSP00000309845.7:n.*36_*61del
ENST00000397594.5:c.*283_*308del (HRAS) ENSP00000380722.1:n.*283_*308del
ENST00000397596.6:c.*144_*169del (HRAS) ENSP00000380723.2:n.*144_*169del
ENST00000417302.5:c.*283_*308del (HRAS) ENSP00000388246.1:n.*283_*308del
ENST00000451590.5:c.*144_*169del (HRAS) ENSP00000407586.1:n.*144_*169del
ENST00000462734.1:n.381_406del (HRAS)
ENST00000478324.5:n.381_406del (HRAS)
ENST00000493230.5:c.*175_*200del (HRAS) ENSP00000434023.1:n.*175_*200del
NM_001130442.1:c.*144_*169del (HRAS) NP_001123914.1:n.*144_*169del
NM_005343.2:c.*36_*61del (HRAS) NP_005334.1:n.*36_*61del
NM_176795.3:c.*283_*308del (HRAS) NP_789765.1:n.*283_*308del
XM_011519875.1:c.-425+4131_-425+4156del (LRRC56) XP_011518177.1:n.-425+4131_-425+4156del
XM_011519877.1:c.-162+4131_-162+4156del (LRRC56) XP_011518179.1:n.-162+4131_-162+4156del
XR_242795.1:n.887_912del (HRAS)
NM_001130442.2:c.*144_*169del (HRAS) NP_001123914.1:n.*144_*169del
NM_001318054.1:c.*36_*61del (HRAS) NP_001304983.1:n.*36_*61del
NM_005343.3:c.*36_*61del (HRAS) NP_005334.1:n.*36_*61del
NM_176795.4:c.*283_*308del (HRAS) NP_789765.1:n.*283_*308del
XM_011519875.2:c.-425+4131_-425+4156del (LRRC56) XP_011518177.1:n.-425+4131_-425+4156del
XM_011519877.2:c.-162+4131_-162+4156del (LRRC56) XP_011518179.1:n.-162+4131_-162+4156del
XM_017017167.1:c.-500+4131_-500+4156del (LRRC56) XP_016872656.1:n.-500+4131_-500+4156del
XM_017017168.1:c.-500+4131_-500+4156del (LRRC56) XP_016872657.1:n.-500+4131_-500+4156del
NM_005343.4:c.*36_*61del (HRAS) MANE Select NP_005334.1:n.*36_*61del
NM_001318054.2:c.*36_*61del (HRAS) NP_001304983.1:n.*36_*61del
NM_001130442.3:c.*144_*169del (HRAS) NP_001123914.1:n.*144_*169del
NM_176795.5:c.*283_*308del (HRAS) MANE Plus Clinical NP_789765.1:n.*283_*308del
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