Canonical Allele Identifier: CA1947140970
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

dbSNP Id: rs1851171547
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532625_532626insTGGGAGTCC , CM000673.2:g.532625_532626insTGGGAGTCC GRCh38
NC_000011.9:g.532625_532626insTGGGAGTCC , CM000673.1:g.532625_532626insTGGGAGTCC GRCh37
NC_000011.8:g.522625_522626insTGGGAGTCC NCBI36
NG_007666.1:g.7927_7928insACTCCCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*26_*27insACTCCCAGG (HRAS) ENSP00000380722.3:n.*26_*27insACTCCCAGG
ENST00000417302.7:c.*151_*152insACTCCCAGG (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*151_*152insACTCCCAGG
ENST00000397594.6:c.257_258insACTCCCAGG (HRAS) ENSP00000380722.2:n.257_258insACTCCCAGG
ENST00000417302.6:c.*151_*152insACTCCCAGG (HRAS) ENSP00000388246.1:n.*151_*152insACTCCCAGG
ENST00000462734.2:c.*187+7_*187+8insACTCCCAGG (HRAS) ENSP00000507303.1:n.*187+7_*187+8insACTCCCAGG
ENST00000311189.8:c.*5+7_*5+8insACTCCCAGG (HRAS) MANE Select ENSP00000309845.7:n.*5+7_*5+8insACTCCCAGG
ENST00000311189.7:c.*5+7_*5+8insACTCCCAGG (HRAS) ENSP00000309845.7:n.*5+7_*5+8insACTCCCAGG
ENST00000397594.5:c.*151_*152insACTCCCAGG (HRAS) ENSP00000380722.1:n.*151_*152insACTCCCAGG
ENST00000397596.6:c.*12_*13insACTCCCAGG (HRAS) ENSP00000380723.2:n.*12_*13insACTCCCAGG
ENST00000417302.5:c.*151_*152insACTCCCAGG (HRAS) ENSP00000388246.1:n.*151_*152insACTCCCAGG
ENST00000451590.5:c.*12_*13insACTCCCAGG (HRAS) ENSP00000407586.1:n.*12_*13insACTCCCAGG
ENST00000462734.1:n.350+7_350+8insACTCCCAGG (HRAS)
ENST00000478324.5:n.249_250insACTCCCAGG (HRAS)
ENST00000493230.5:c.*144+7_*144+8insACTCCCAGG (HRAS) ENSP00000434023.1:n.*144+7_*144+8insACTCCCAGG
NM_001130442.1:c.*12_*13insACTCCCAGG (HRAS) NP_001123914.1:n.*12_*13insACTCCCAGG
NM_005343.2:c.*5+7_*5+8insACTCCCAGG (HRAS) NP_005334.1:n.*5+7_*5+8insACTCCCAGG
NM_176795.3:c.*151_*152insACTCCCAGG (HRAS) NP_789765.1:n.*151_*152insACTCCCAGG
XM_011519875.1:c.-425+4288_-425+4289insTGGGAGTCC (LRRC56) XP_011518177.1:n.-425+4288_-425+4289insTGGGAGTCC
XM_011519877.1:c.-162+4288_-162+4289insTGGGAGTCC (LRRC56) XP_011518179.1:n.-162+4288_-162+4289insTGGGAGTCC
XR_242795.1:n.856+7_856+8insACTCCCAGG (HRAS)
NM_001130442.2:c.*12_*13insACTCCCAGG (HRAS) NP_001123914.1:n.*12_*13insACTCCCAGG
NM_001318054.1:c.*5+7_*5+8insACTCCCAGG (HRAS) NP_001304983.1:n.*5+7_*5+8insACTCCCAGG
NM_005343.3:c.*5+7_*5+8insACTCCCAGG (HRAS) NP_005334.1:n.*5+7_*5+8insACTCCCAGG
NM_176795.4:c.*151_*152insACTCCCAGG (HRAS) NP_789765.1:n.*151_*152insACTCCCAGG
XM_011519875.2:c.-425+4288_-425+4289insTGGGAGTCC (LRRC56) XP_011518177.1:n.-425+4288_-425+4289insTGGGAGTCC
XM_011519877.2:c.-162+4288_-162+4289insTGGGAGTCC (LRRC56) XP_011518179.1:n.-162+4288_-162+4289insTGGGAGTCC
XM_017017167.1:c.-500+4288_-500+4289insTGGGAGTCC (LRRC56) XP_016872656.1:n.-500+4288_-500+4289insTGGGAGTCC
XM_017017168.1:c.-500+4288_-500+4289insTGGGAGTCC (LRRC56) XP_016872657.1:n.-500+4288_-500+4289insTGGGAGTCC
NM_005343.4:c.*5+7_*5+8insACTCCCAGG (HRAS) MANE Select NP_005334.1:n.*5+7_*5+8insACTCCCAGG
NM_001318054.2:c.*5+7_*5+8insACTCCCAGG (HRAS) NP_001304983.1:n.*5+7_*5+8insACTCCCAGG
NM_001130442.3:c.*12_*13insACTCCCAGG (HRAS) NP_001123914.1:n.*12_*13insACTCCCAGG
NM_176795.5:c.*151_*152insACTCCCAGG (HRAS) MANE Plus Clinical NP_789765.1:n.*151_*152insACTCCCAGG
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