Canonical Allele Identifier: CA2723264586
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

dbSNP Id: rs2133980961
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532447_532466dup , CM000673.2:g.532447_532466dup GRCh38
NC_000011.9:g.532447_532466dup , CM000673.1:g.532447_532466dup GRCh37
NC_000011.8:g.522447_522466dup NCBI36
NG_007666.1:g.8085_8104dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*184_*203dup (HRAS) ENSP00000380722.3:n.*184_*203dup
ENST00000417302.7:c.*309_*328dup (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*309_*328dup
ENST00000397594.6:c.415_434dup (HRAS) ENSP00000380722.2:n.415_434dup
ENST00000417302.6:c.*309_*328dup (HRAS) ENSP00000388246.1:n.*309_*328dup
ENST00000462734.2:c.*244_*263dup (HRAS) ENSP00000507303.1:n.*244_*263dup
ENST00000311189.8:c.*62_*81dup (HRAS) MANE Select ENSP00000309845.7:n.*62_*81dup
ENST00000311189.7:c.*62_*81dup (HRAS) ENSP00000309845.7:n.*62_*81dup
ENST00000397594.5:c.*309_*328dup (HRAS) ENSP00000380722.1:n.*309_*328dup
ENST00000397596.6:c.*170_*189dup (HRAS) ENSP00000380723.2:n.*170_*189dup
ENST00000417302.5:c.*309_*328dup (HRAS) ENSP00000388246.1:n.*309_*328dup
ENST00000451590.5:c.*170_*189dup (HRAS) ENSP00000407586.1:n.*170_*189dup
ENST00000462734.1:n.407_426dup (HRAS)
ENST00000478324.5:n.407_426dup (HRAS)
ENST00000493230.5:c.*201_*220dup (HRAS) ENSP00000434023.1:n.*201_*220dup
NM_001130442.1:c.*170_*189dup (HRAS) NP_001123914.1:n.*170_*189dup
NM_005343.2:c.*62_*81dup (HRAS) NP_005334.1:n.*62_*81dup
NM_176795.3:c.*309_*328dup (HRAS) NP_789765.1:n.*309_*328dup
XM_011519875.1:c.-425+4110_-425+4129dup (LRRC56) XP_011518177.1:n.-425+4110_-425+4129dup
XM_011519877.1:c.-162+4110_-162+4129dup (LRRC56) XP_011518179.1:n.-162+4110_-162+4129dup
XR_242795.1:n.913_932dup (HRAS)
NM_001130442.2:c.*170_*189dup (HRAS) NP_001123914.1:n.*170_*189dup
NM_001318054.1:c.*62_*81dup (HRAS) NP_001304983.1:n.*62_*81dup
NM_005343.3:c.*62_*81dup (HRAS) NP_005334.1:n.*62_*81dup
NM_176795.4:c.*309_*328dup (HRAS) NP_789765.1:n.*309_*328dup
XM_011519875.2:c.-425+4110_-425+4129dup (LRRC56) XP_011518177.1:n.-425+4110_-425+4129dup
XM_011519877.2:c.-162+4110_-162+4129dup (LRRC56) XP_011518179.1:n.-162+4110_-162+4129dup
XM_017017167.1:c.-500+4110_-500+4129dup (LRRC56) XP_016872656.1:n.-500+4110_-500+4129dup
XM_017017168.1:c.-500+4110_-500+4129dup (LRRC56) XP_016872657.1:n.-500+4110_-500+4129dup
NM_005343.4:c.*62_*81dup (HRAS) MANE Select NP_005334.1:n.*62_*81dup
NM_001318054.2:c.*62_*81dup (HRAS) NP_001304983.1:n.*62_*81dup
NM_001130442.3:c.*170_*189dup (HRAS) NP_001123914.1:n.*170_*189dup
NM_176795.5:c.*309_*328dup (HRAS) MANE Plus Clinical NP_789765.1:n.*309_*328dup
Search 100 bp 5'
Search 100 bp 3'