Linked Data
dbSNP Id:
rs1313411661
gnomAD v3:
11-532478-T-TGCACCTCCTTCCTGCATCCG
gnomAD v4:
11-532478-T-TGCACCTCCTTCCTGCATCCG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.532487_532506dup , CM000673.2:g.532487_532506dup | GRCh38 |
| NC_000011.9:g.532487_532506dup , CM000673.1:g.532487_532506dup | GRCh37 |
| NC_000011.8:g.522487_522506dup | NCBI36 |
| NG_007666.1:g.8053_8072dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.*152_*171dup (HRAS) | ENSP00000380722.3:n.*152_*171dup | |
| ENST00000417302.7:c.*277_*296dup (HRAS) MANE Plus Clinical | ENSP00000388246.1:n.*277_*296dup | |
| ENST00000397594.6:c.383_402dup (HRAS) | ENSP00000380722.2:n.383_402dup | |
| ENST00000417302.6:c.*277_*296dup (HRAS) | ENSP00000388246.1:n.*277_*296dup | |
| ENST00000462734.2:c.*212_*231dup (HRAS) | ENSP00000507303.1:n.*212_*231dup | |
| ENST00000311189.8:c.*30_*49dup (HRAS) MANE Select | ENSP00000309845.7:n.*30_*49dup | |
| ENST00000311189.7:c.*30_*49dup (HRAS) | ENSP00000309845.7:n.*30_*49dup | |
| ENST00000397594.5:c.*277_*296dup (HRAS) | ENSP00000380722.1:n.*277_*296dup | |
| ENST00000397596.6:c.*138_*157dup (HRAS) | ENSP00000380723.2:n.*138_*157dup | |
| ENST00000417302.5:c.*277_*296dup (HRAS) | ENSP00000388246.1:n.*277_*296dup | |
| ENST00000451590.5:c.*138_*157dup (HRAS) | ENSP00000407586.1:n.*138_*157dup | |
| ENST00000462734.1:n.375_394dup (HRAS) | ||
| ENST00000478324.5:n.375_394dup (HRAS) | ||
| ENST00000493230.5:c.*169_*188dup (HRAS) | ENSP00000434023.1:n.*169_*188dup | |
| NM_001130442.1:c.*138_*157dup (HRAS) | NP_001123914.1:n.*138_*157dup | |
| NM_005343.2:c.*30_*49dup (HRAS) | NP_005334.1:n.*30_*49dup | |
| NM_176795.3:c.*277_*296dup (HRAS) | NP_789765.1:n.*277_*296dup | |
| XM_011519875.1:c.-425+4150_-425+4169dup (LRRC56) | XP_011518177.1:n.-425+4150_-425+4169dup | |
| XM_011519877.1:c.-162+4150_-162+4169dup (LRRC56) | XP_011518179.1:n.-162+4150_-162+4169dup | |
| XR_242795.1:n.881_900dup (HRAS) | ||
| NM_001130442.2:c.*138_*157dup (HRAS) | NP_001123914.1:n.*138_*157dup | |
| NM_001318054.1:c.*30_*49dup (HRAS) | NP_001304983.1:n.*30_*49dup | |
| NM_005343.3:c.*30_*49dup (HRAS) | NP_005334.1:n.*30_*49dup | |
| NM_176795.4:c.*277_*296dup (HRAS) | NP_789765.1:n.*277_*296dup | |
| XM_011519875.2:c.-425+4150_-425+4169dup (LRRC56) | XP_011518177.1:n.-425+4150_-425+4169dup | |
| XM_011519877.2:c.-162+4150_-162+4169dup (LRRC56) | XP_011518179.1:n.-162+4150_-162+4169dup | |
| XM_017017167.1:c.-500+4150_-500+4169dup (LRRC56) | XP_016872656.1:n.-500+4150_-500+4169dup | |
| XM_017017168.1:c.-500+4150_-500+4169dup (LRRC56) | XP_016872657.1:n.-500+4150_-500+4169dup | |
| NM_005343.4:c.*30_*49dup (HRAS) MANE Select | NP_005334.1:n.*30_*49dup | |
| NM_001318054.2:c.*30_*49dup (HRAS) | NP_001304983.1:n.*30_*49dup | |
| NM_001130442.3:c.*138_*157dup (HRAS) | NP_001123914.1:n.*138_*157dup | |
| NM_176795.5:c.*277_*296dup (HRAS) MANE Plus Clinical | NP_789765.1:n.*277_*296dup |