Canonical Allele Identifier: CA677772822
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

dbSNP Id: rs1273622267
gnomAD v3: 11-532607-GGCC-G
gnomAD v4: 11-532607-GGCC-G
MyVariant Identifiers: chr11:g.532608_532610del (hg19) chr11:g.532608_532610del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532611_532613del , CM000673.2:g.532611_532613del GRCh38
NC_000011.9:g.532611_532613del , CM000673.1:g.532611_532613del GRCh37
NC_000011.8:g.522611_522613del NCBI36
NG_007666.1:g.7941_7943del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*40_*42del (HRAS) ENSP00000380722.3:n.*40_*42del
ENST00000417302.7:c.*165_*167del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*165_*167del
ENST00000397594.6:c.271_273del (HRAS) ENSP00000380722.2:n.271_273del
ENST00000417302.6:c.*165_*167del (HRAS) ENSP00000388246.1:n.*165_*167del
ENST00000462734.2:c.*187+21_*187+23del (HRAS) ENSP00000507303.1:n.*187+21_*187+23del
ENST00000311189.8:c.*5+21_*5+23del (HRAS) MANE Select ENSP00000309845.7:n.*5+21_*5+23del
ENST00000311189.7:c.*5+21_*5+23del (HRAS) ENSP00000309845.7:n.*5+21_*5+23del
ENST00000397594.5:c.*165_*167del (HRAS) ENSP00000380722.1:n.*165_*167del
ENST00000397596.6:c.*26_*28del (HRAS) ENSP00000380723.2:n.*26_*28del
ENST00000417302.5:c.*165_*167del (HRAS) ENSP00000388246.1:n.*165_*167del
ENST00000451590.5:c.*26_*28del (HRAS) ENSP00000407586.1:n.*26_*28del
ENST00000462734.1:n.350+21_350+23del (HRAS)
ENST00000478324.5:n.263_265del (HRAS)
ENST00000493230.5:c.*144+21_*144+23del (HRAS) ENSP00000434023.1:n.*144+21_*144+23del
NM_001130442.1:c.*26_*28del (HRAS) NP_001123914.1:n.*26_*28del
NM_005343.2:c.*5+21_*5+23del (HRAS) NP_005334.1:n.*5+21_*5+23del
NM_176795.3:c.*165_*167del (HRAS) NP_789765.1:n.*165_*167del
XM_011519875.1:c.-425+4274_-425+4276del (LRRC56) XP_011518177.1:n.-425+4274_-425+4276del
XM_011519877.1:c.-162+4274_-162+4276del (LRRC56) XP_011518179.1:n.-162+4274_-162+4276del
XR_242795.1:n.856+21_856+23del (HRAS)
NM_001130442.2:c.*26_*28del (HRAS) NP_001123914.1:n.*26_*28del
NM_001318054.1:c.*5+21_*5+23del (HRAS) NP_001304983.1:n.*5+21_*5+23del
NM_005343.3:c.*5+21_*5+23del (HRAS) NP_005334.1:n.*5+21_*5+23del
NM_176795.4:c.*165_*167del (HRAS) NP_789765.1:n.*165_*167del
XM_011519875.2:c.-425+4274_-425+4276del (LRRC56) XP_011518177.1:n.-425+4274_-425+4276del
XM_011519877.2:c.-162+4274_-162+4276del (LRRC56) XP_011518179.1:n.-162+4274_-162+4276del
XM_017017167.1:c.-500+4274_-500+4276del (LRRC56) XP_016872656.1:n.-500+4274_-500+4276del
XM_017017168.1:c.-500+4274_-500+4276del (LRRC56) XP_016872657.1:n.-500+4274_-500+4276del
NM_005343.4:c.*5+21_*5+23del (HRAS) MANE Select NP_005334.1:n.*5+21_*5+23del
NM_001318054.2:c.*5+21_*5+23del (HRAS) NP_001304983.1:n.*5+21_*5+23del
NM_001130442.3:c.*26_*28del (HRAS) NP_001123914.1:n.*26_*28del
NM_176795.5:c.*165_*167del (HRAS) MANE Plus Clinical NP_789765.1:n.*165_*167del
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