Linked Data
gnomAD v2:
22-19711726-GC-G
gnomAD v4:
22-19724203-GC-G
MyVariant Identifiers:
chr22:g.19711727del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19724208del , CM000684.2:g.19724208del | GRCh38 |
| NC_000022.10:g.19711731del , CM000684.1:g.19711731del | GRCh37 |
| NC_000022.9:g.18091731del | NCBI36 |
| NG_007974.1:g.5666del , LRG_478:g.5666del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366425.4:c.365del (GP1BB) MANE Select | ENSP00000383382.2:p.Pro122GlnfsTer? | |
| ENST00000366425.3:c.365del (GP1BB) | ENSP00000383382.2:p.Pro122GlnfsTer? | |
| ENST00000431044.5:c.*1450del (SEPTIN5) | ENSP00000399685.1:n.*1450del | |
| ENST00000455843.5:c.*1450del (SEPTIN5) | ENSP00000391731.1:n.*1450del | |
| ENST00000470814.1:n.2337del (SEPTIN5) | ||
| NM_000407.4:c.365del , LRG_478t1:c.365del (GP1BB) | NP_000398.1:p.Pro122GlnfsTer? | |
| NR_037611.1:n.4105del | ||
| NR_037612.1:n.2609del | ||
| NM_000407.5:c.365del (GP1BB) MANE Select | NP_000398.1:p.Pro122GlnfsTer? |