Linked Data
dbSNP Id:
rs757189431
ExAC:
1:43804430 GC / G
gnomAD v2:
1-43804430-GC-G
gnomAD v4:
1-43338759-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.43338760del , CM000663.2:g.43338760del | GRCh38 |
| NC_000001.10:g.43804431del , CM000663.1:g.43804431del | GRCh37 |
| NC_000001.9:g.43577018del | NCBI36 |
| NG_007525.1:g.5957del , LRG_510:g.5957del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372470.9:c.391+40del MANE Select | ENSP00000361548.3:n.391+40del | |
| ENST00000413998.7:c.370+40del | ENSP00000414004.3:n.370+40del | |
| ENST00000638732.1:n.391+40del | ||
| ENST00000372470.7:c.391+40del | ENSP00000361548.3:n.391+40del | |
| ENST00000413998.6:c.391+40del | ENSP00000414004.2:n.391+40del | |
| ENST00000612993.1:c.391+40del | ENSP00000480273.1:n.391+40del | |
| NM_005373.2:c.391+40del , LRG_510t1:c.391+40del | NP_005364.1:n.391+40del | |
| XM_011541478.1:c.370+40del | XP_011539780.1:n.370+40del | |
| XM_017001320.1:c.562+40del | XP_016856809.1:n.562+40del | |
| NM_005373.3:c.391+40del MANE Select | NP_005364.1:n.391+40del |