Linked Data
ClinVar Variation Id:
420858
dbSNP Id:
rs763938484
ExAC:
8:90982581 T / TA
gnomAD v2:
8-90982581-T-TA
gnomAD v3:
8-89970353-T-TA
gnomAD v4:
8-89970353-T-TA
COSMIC:
COSN17142905
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.89970355dup , CM000670.2:g.89970355dup | GRCh38 |
| NC_000008.10:g.90982583dup , CM000670.1:g.90982583dup | GRCh37 |
| NC_000008.9:g.91051759dup | NCBI36 |
| NG_008860.1:g.19318dup , LRG_158:g.19318dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494804.2:n.2198+10dup | ||
| ENST00000517337.2:c.650+10dup | ENSP00000429971.2:n.650+10dup | |
| ENST00000523444.2:c.650+10dup | ENSP00000428252.2:n.650+10dup | |
| ENST00000697292.1:c.896+10dup | ENSP00000513229.1:n.896+10dup | |
| ENST00000697293.1:c.896+10dup | ENSP00000513230.1:n.896+10dup | |
| ENST00000697294.1:c.*507+10dup | ENSP00000513231.1:n.*507+10dup | |
| ENST00000697295.1:c.*205+10dup | ENSP00000513232.1:n.*205+10dup | |
| ENST00000697296.1:c.*564+10dup | ENSP00000513233.1:n.*564+10dup | |
| ENST00000697297.1:n.2681+10dup | ||
| ENST00000697298.1:c.650+10dup | ENSP00000513234.1:n.650+10dup | |
| ENST00000697299.1:c.650+10dup | ENSP00000513235.1:n.650+10dup | |
| ENST00000697300.1:c.*500+10dup | ENSP00000513236.1:n.*500+10dup | |
| ENST00000697301.1:c.*417+10dup | ENSP00000513237.1:n.*417+10dup | |
| ENST00000697302.1:c.*417+10dup | ENSP00000513238.1:n.*417+10dup | |
| ENST00000697303.1:c.*500+10dup | ENSP00000513239.1:n.*500+10dup | |
| ENST00000697304.1:c.585-5847dup | ENSP00000513240.1:n.585-5847dup | |
| ENST00000697306.1:c.480+10380dup | ENSP00000513241.1:n.480+10380dup | |
| ENST00000697307.1:c.896+10dup | ENSP00000513242.1:n.896+10dup | |
| ENST00000697308.1:c.896+10dup | ENSP00000513243.1:n.896+10dup | |
| ENST00000697309.1:c.896+10dup | ENSP00000513244.1:n.896+10dup | |
| ENST00000697310.1:c.896+10dup | ENSP00000513245.1:n.896+10dup | |
| ENST00000697311.1:c.896+10dup | ENSP00000513246.1:n.896+10dup | |
| ENST00000697312.1:c.*294+10dup | ENSP00000513247.1:n.*294+10dup | |
| ENST00000697313.1:n.2687+10dup | ||
| ENST00000697314.1:n.2687+10dup | ||
| ENST00000697315.1:c.896+10dup | ENSP00000513248.1:n.896+10dup | |
| ENST00000697316.1:n.1017+10dup | ||
| ENST00000697317.1:n.1006+10dup | ||
| ENST00000697318.1:n.1008+10dup | ||
| ENST00000265433.8:c.896+10dup MANE Select | ENSP00000265433.4:n.896+10dup | |
| ENST00000265433.7:c.896+10dup | ENSP00000265433.3:n.896+10dup | |
| ENST00000396252.6:c.*769+10dup | ENSP00000379551.2:n.*769+10dup | |
| ENST00000409330.5:c.650+10dup | ENSP00000386924.1:n.650+10dup | |
| NM_001024688.2:c.650+10dup | NP_001019859.1:n.650+10dup | |
| NM_002485.4:c.896+10dup , LRG_158t1:c.896+10dup | NP_002476.2:n.896+10dup | |
| XM_011517044.1:c.872+10dup | XP_011515346.1:n.872+10dup | |
| XM_011517045.1:c.650+10dup | XP_011515347.1:n.650+10dup | |
| XM_011517046.1:c.896+10dup | XP_011515348.1:n.896+10dup | |
| XR_928335.1:n.1033+10dup | ||
| XM_017013460.1:c.17+10dup | XP_016868949.1:n.17+10dup | |
| XM_017013462.2:c.17+10dup | XP_016868951.1:n.17+10dup | |
| XM_024447163.1:c.650+10dup | XP_024302931.1:n.650+10dup | |
| XM_024447164.1:c.650+10dup | XP_024302932.1:n.650+10dup | |
| XM_024447165.1:c.17+10dup | XP_024302933.1:n.17+10dup | |
| NM_002485.5:c.896+10dup MANE Select | NP_002476.2:n.896+10dup | |
| NM_001024688.3:c.650+10dup | NP_001019859.1:n.650+10dup |