Linked Data
dbSNP Id:
rs760177349
ExAC:
8:94793089 TA / T
gnomAD v2:
8-94793089-TA-T
gnomAD v3:
8-93780861-TA-T
gnomAD v4:
8-93780861-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.93780863del , CM000670.2:g.93780863del | GRCh38 |
| NC_000008.10:g.94793091del , CM000670.1:g.94793091del | GRCh37 |
| NC_000008.9:g.94862267del | NCBI36 |
| NG_009190.1:g.31020del , LRG_688:g.31020del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000323130.8:c.870-11del | ENSP00000314488.4:n.870-11del | |
| ENST00000409623.8:c.870-11del | ENSP00000386966.4:n.870-11del | |
| ENST00000452276.6:c.870-11del | ENSP00000388671.2:n.870-11del | |
| ENST00000453906.6:c.407-5360del | ENSP00000403035.2:n.407-5360del | |
| ENST00000520680.2:c.870-11del | ENSP00000428785.2:n.870-11del | |
| ENST00000521065.2:c.*587-11del | ENSP00000427947.2:n.*587-11del | |
| ENST00000521517.6:c.870-11del | ENSP00000430740.2:n.870-11del | |
| ENST00000681998.1:c.799+116del | ENSP00000506773.1:n.799+116del | |
| ENST00000682036.1:c.407-5360del | ENSP00000508390.1:n.407-5360del | |
| ENST00000682577.1:c.800-11del | ENSP00000506963.1:n.800-11del | |
| ENST00000682624.1:c.*444-11del | ENSP00000508343.1:n.*444-11del | |
| ENST00000682700.1:c.870-11del | ENSP00000507627.1:n.870-11del | |
| ENST00000682744.1:n.408-11del | ||
| ENST00000682804.1:n.693-11del | ||
| ENST00000682837.1:c.624+116del | ENSP00000507920.1:n.624+116del | |
| ENST00000682935.1:n.2430-11del | ||
| ENST00000682984.1:c.531-11del | ENSP00000507209.1:n.531-11del | |
| ENST00000683078.1:c.625-11del | ENSP00000506796.1:n.625-11del | |
| ENST00000683223.1:c.710+116del | ENSP00000507685.1:n.710+116del | |
| ENST00000683238.1:n.2251-11del | ||
| ENST00000683249.1:n.2456del | ||
| ENST00000683336.1:c.799+116del | ENSP00000507695.1:n.799+116del | |
| ENST00000683362.1:c.531-11del | ENSP00000506985.1:n.531-11del | |
| ENST00000683850.1:n.793-11del | ||
| ENST00000683919.1:c.800-11del | ENSP00000507617.1:n.800-11del | |
| ENST00000683953.1:c.781-11del | ENSP00000508375.1:n.781-11del | |
| ENST00000684023.1:c.1004-11del | ENSP00000507461.1:n.1004-11del | |
| ENST00000684064.1:c.561-11del | ENSP00000508192.1:n.561-11del | |
| ENST00000684089.1:n.2420-11del | ||
| ENST00000684149.1:c.*206-11del | ENSP00000507943.1:n.*206-11del | |
| ENST00000684416.1:n.829-11del | ||
| ENST00000684540.1:c.800-11del | ENSP00000507987.1:n.800-11del | |
| ENST00000453321.8:c.870-11del MANE Select | ENSP00000389998.3:n.870-11del | |
| ENST00000323130.7:c.840-11del | ENSP00000314488.3:n.840-11del | |
| ENST00000409623.7:c.627-11del | ENSP00000386966.3:n.627-11del | |
| ENST00000425545.2:n.317-11del | ||
| ENST00000452276.5:c.561-11del | ENSP00000388671.1:n.561-11del | |
| ENST00000453321.7:c.870-11del | ENSP00000389998.3:n.870-11del | |
| ENST00000453906.5:c.407-5360del | ENSP00000403035.1:n.407-5360del | |
| ENST00000474944.5:n.427-5360del | ||
| ENST00000496213.5:n.335-11del | ||
| NM_001142301.1:c.627-11del , LRG_688t2:c.627-11del | NP_001135773.1:n.627-11del | |
| NM_153704.5:c.870-11del , LRG_688t1:c.870-11del | NP_714915.3:n.870-11del | |
| NR_024522.1:n.941-11del | ||
| XM_006716686.2:c.567-11del | XP_006716749.1:n.567-11del | |
| XM_006716687.2:c.270-11del | XP_006716750.1:n.270-11del | |
| XM_011517363.1:c.407-5360del | XP_011515665.1:n.407-5360del | |
| XR_428387.1:n.928-11del | ||
| XR_928360.1:n.928-11del | ||
| XR_928361.1:n.928-11del | ||
| XR_928362.1:n.928-11del | ||
| XM_006716686.4:c.567-11del | XP_006716749.1:n.567-11del | |
| XM_011517363.3:c.407-5360del | XP_011515665.1:n.407-5360del | |
| XM_024447326.1:c.216-11del | XP_024303094.1:n.216-11del | |
| XR_001745619.2:n.911-11del | ||
| XR_428387.2:n.911-11del | ||
| XR_928360.3:n.911-11del | ||
| XR_928362.3:n.911-11del | ||
| NM_153704.6:c.870-11del MANE Select | NP_714915.3:n.870-11del | |
| NR_024522.2:n.891-11del |