Linked Data
dbSNP Id:
rs1436500174
gnomAD v3:
11-532481-A-ACCTCCTT
gnomAD v4:
11-532481-A-ACCTCCTT
MyVariant Identifiers:
chr11:g.532481_532482insCCTCCTT (hg19)
chr11:g.532481_532482insCCTCCTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.532485_532491dup , CM000673.2:g.532485_532491dup | GRCh38 |
| NC_000011.9:g.532485_532491dup , CM000673.1:g.532485_532491dup | GRCh37 |
| NC_000011.8:g.522485_522491dup | NCBI36 |
| NG_007666.1:g.8063_8069dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.*162_*168dup (HRAS) | ENSP00000380722.3:n.*162_*168dup | |
| ENST00000417302.7:c.*287_*293dup (HRAS) MANE Plus Clinical | ENSP00000388246.1:n.*287_*293dup | |
| ENST00000397594.6:c.393_399dup (HRAS) | ENSP00000380722.2:n.393_399dup | |
| ENST00000417302.6:c.*287_*293dup (HRAS) | ENSP00000388246.1:n.*287_*293dup | |
| ENST00000462734.2:c.*222_*228dup (HRAS) | ENSP00000507303.1:n.*222_*228dup | |
| ENST00000311189.8:c.*40_*46dup (HRAS) MANE Select | ENSP00000309845.7:n.*40_*46dup | |
| ENST00000311189.7:c.*40_*46dup (HRAS) | ENSP00000309845.7:n.*40_*46dup | |
| ENST00000397594.5:c.*287_*293dup (HRAS) | ENSP00000380722.1:n.*287_*293dup | |
| ENST00000397596.6:c.*148_*154dup (HRAS) | ENSP00000380723.2:n.*148_*154dup | |
| ENST00000417302.5:c.*287_*293dup (HRAS) | ENSP00000388246.1:n.*287_*293dup | |
| ENST00000451590.5:c.*148_*154dup (HRAS) | ENSP00000407586.1:n.*148_*154dup | |
| ENST00000462734.1:n.385_391dup (HRAS) | ||
| ENST00000478324.5:n.385_391dup (HRAS) | ||
| ENST00000493230.5:c.*179_*185dup (HRAS) | ENSP00000434023.1:n.*179_*185dup | |
| NM_001130442.1:c.*148_*154dup (HRAS) | NP_001123914.1:n.*148_*154dup | |
| NM_005343.2:c.*40_*46dup (HRAS) | NP_005334.1:n.*40_*46dup | |
| NM_176795.3:c.*287_*293dup (HRAS) | NP_789765.1:n.*287_*293dup | |
| XM_011519875.1:c.-425+4148_-425+4154dup (LRRC56) | XP_011518177.1:n.-425+4148_-425+4154dup | |
| XM_011519877.1:c.-162+4148_-162+4154dup (LRRC56) | XP_011518179.1:n.-162+4148_-162+4154dup | |
| XR_242795.1:n.891_897dup (HRAS) | ||
| NM_001130442.2:c.*148_*154dup (HRAS) | NP_001123914.1:n.*148_*154dup | |
| NM_001318054.1:c.*40_*46dup (HRAS) | NP_001304983.1:n.*40_*46dup | |
| NM_005343.3:c.*40_*46dup (HRAS) | NP_005334.1:n.*40_*46dup | |
| NM_176795.4:c.*287_*293dup (HRAS) | NP_789765.1:n.*287_*293dup | |
| XM_011519875.2:c.-425+4148_-425+4154dup (LRRC56) | XP_011518177.1:n.-425+4148_-425+4154dup | |
| XM_011519877.2:c.-162+4148_-162+4154dup (LRRC56) | XP_011518179.1:n.-162+4148_-162+4154dup | |
| XM_017017167.1:c.-500+4148_-500+4154dup (LRRC56) | XP_016872656.1:n.-500+4148_-500+4154dup | |
| XM_017017168.1:c.-500+4148_-500+4154dup (LRRC56) | XP_016872657.1:n.-500+4148_-500+4154dup | |
| NM_005343.4:c.*40_*46dup (HRAS) MANE Select | NP_005334.1:n.*40_*46dup | |
| NM_001318054.2:c.*40_*46dup (HRAS) | NP_001304983.1:n.*40_*46dup | |
| NM_001130442.3:c.*148_*154dup (HRAS) | NP_001123914.1:n.*148_*154dup | |
| NM_176795.5:c.*287_*293dup (HRAS) MANE Plus Clinical | NP_789765.1:n.*287_*293dup |