Canonical Allele Identifier: CA2611691683
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

gnomAD v4: 11-532567-CGGCAGGGGCGG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532570_532580del , CM000673.2:g.532570_532580del GRCh38
NC_000011.9:g.532570_532580del , CM000673.1:g.532570_532580del GRCh37
NC_000011.8:g.522570_522580del NCBI36
NG_007666.1:g.7973_7983del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*72_*82del (HRAS) ENSP00000380722.3:n.*72_*82del
ENST00000417302.7:c.*197_*207del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*197_*207del
ENST00000397594.6:c.303_313del (HRAS) ENSP00000380722.2:n.303_313del
ENST00000417302.6:c.*197_*207del (HRAS) ENSP00000388246.1:n.*197_*207del
ENST00000462734.2:c.*187+53_*188-46del (HRAS) ENSP00000507303.1:n.*187+53_*188-46del
ENST00000311189.8:c.*5+53_*6-46del (HRAS) MANE Select ENSP00000309845.7:n.*5+53_*6-46del
ENST00000311189.7:c.*5+53_*6-46del (HRAS) ENSP00000309845.7:n.*5+53_*6-46del
ENST00000397594.5:c.*197_*207del (HRAS) ENSP00000380722.1:n.*197_*207del
ENST00000397596.6:c.*58_*68del (HRAS) ENSP00000380723.2:n.*58_*68del
ENST00000417302.5:c.*197_*207del (HRAS) ENSP00000388246.1:n.*197_*207del
ENST00000451590.5:c.*58_*68del (HRAS) ENSP00000407586.1:n.*58_*68del
ENST00000462734.1:n.350+53_351-46del (HRAS)
ENST00000478324.5:n.295_305del (HRAS)
ENST00000493230.5:c.*144+53_*145-46del (HRAS) ENSP00000434023.1:n.*144+53_*145-46del
NM_001130442.1:c.*58_*68del (HRAS) NP_001123914.1:n.*58_*68del
NM_005343.2:c.*5+53_*6-46del (HRAS) NP_005334.1:n.*5+53_*6-46del
NM_176795.3:c.*197_*207del (HRAS) NP_789765.1:n.*197_*207del
XM_011519875.1:c.-425+4233_-425+4243del (LRRC56) XP_011518177.1:n.-425+4233_-425+4243del
XM_011519877.1:c.-162+4233_-162+4243del (LRRC56) XP_011518179.1:n.-162+4233_-162+4243del
XR_242795.1:n.856+53_857-46del (HRAS)
NM_001130442.2:c.*58_*68del (HRAS) NP_001123914.1:n.*58_*68del
NM_001318054.1:c.*5+53_*6-46del (HRAS) NP_001304983.1:n.*5+53_*6-46del
NM_005343.3:c.*5+53_*6-46del (HRAS) NP_005334.1:n.*5+53_*6-46del
NM_176795.4:c.*197_*207del (HRAS) NP_789765.1:n.*197_*207del
XM_011519875.2:c.-425+4233_-425+4243del (LRRC56) XP_011518177.1:n.-425+4233_-425+4243del
XM_011519877.2:c.-162+4233_-162+4243del (LRRC56) XP_011518179.1:n.-162+4233_-162+4243del
XM_017017167.1:c.-500+4233_-500+4243del (LRRC56) XP_016872656.1:n.-500+4233_-500+4243del
XM_017017168.1:c.-500+4233_-500+4243del (LRRC56) XP_016872657.1:n.-500+4233_-500+4243del
NM_005343.4:c.*5+53_*6-46del (HRAS) MANE Select NP_005334.1:n.*5+53_*6-46del
NM_001318054.2:c.*5+53_*6-46del (HRAS) NP_001304983.1:n.*5+53_*6-46del
NM_001130442.3:c.*58_*68del (HRAS) NP_001123914.1:n.*58_*68del
NM_176795.5:c.*197_*207del (HRAS) MANE Plus Clinical NP_789765.1:n.*197_*207del
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