Linked Data
dbSNP Id:
rs1491181768
gnomAD v2:
4-122607182-TGC-T
gnomAD v3:
4-121686027-TGC-T
gnomAD v4:
4-121686027-TGC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121686028_121686029del , CM000666.2:g.121686028_121686029del | GRCh38 |
| NC_000004.11:g.122607183_122607184del , CM000666.1:g.122607183_122607184del | GRCh37 |
| NC_000004.10:g.122826633_122826634del | NCBI36 |
| NG_032042.1:g.15964_15965del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296511.10:c.94+259_94+260del MANE Select | ENSP00000296511.5:n.94+259_94+260del | |
| ENST00000296511.9:c.94+259_94+260del | ENSP00000296511.5:n.94+259_94+260del | |
| ENST00000501272.6:c.10-2552_10-2551del | ENSP00000424106.1:n.10-2552_10-2551del | |
| ENST00000506395.5:c.94+259_94+260del | ENSP00000421421.1:n.94+259_94+260del | |
| ENST00000509016.5:n.215+259_215+260del | ||
| ENST00000511552.5:n.480+259_480+260del | ||
| ENST00000513428.5:n.259+259_259+260del | ||
| ENST00000513523.1:n.262+259_262+260del | ||
| ENST00000513728.1:c.94+259_94+260del | ENSP00000427135.1:n.94+259_94+260del | |
| ENST00000515017.5:c.94+259_94+260del | ENSP00000424199.1:n.94+259_94+260del | |
| NM_001154.3:c.94+259_94+260del | NP_001145.1:n.94+259_94+260del | |
| XM_017008141.2:c.94+259_94+260del | XP_016863630.1:n.94+259_94+260del | |
| NM_001154.4:c.94+259_94+260del MANE Select | NP_001145.1:n.94+259_94+260del |