Linked Data
dbSNP Id:
rs774071527
ExAC:
17:61995319 CG / C
gnomAD v2:
17-61995319-CG-C
gnomAD v3:
17-63917959-CG-C
gnomAD v4:
17-63917959-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63917964del , CM000679.2:g.63917964del | GRCh38 |
| NC_000017.10:g.61995324del , CM000679.1:g.61995324del | GRCh37 |
| NC_000017.9:g.59349056del | NCBI36 |
| NG_011676.1:g.5879del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323322.10:c.292-36del (GH1) MANE Select | ENSP00000312673.5:n.292-36del | |
| ENST00000647774.1:c.570-36del | ||
| ENST00000323322.9:c.292-36del (GH1) | ENSP00000312673.5:n.292-36del | |
| ENST00000342364.8:c.171+386del (GH1) | ENSP00000339278.4:n.171+386del | |
| ENST00000351388.8:c.172-36del (GH1) | ENSP00000343791.4:n.172-36del | |
| ENST00000392824.8:c.10+807del (CSHL1) | ENSP00000376569.5:n.10+807del | |
| ENST00000458650.6:c.247-36del (GH1) | ENSP00000408486.2:n.247-36del | |
| ENST00000579711.1:n.653-36del (GH1) | ||
| ENST00000617086.1:c.11-454del (GH1) | ENSP00000481276.1:n.11-454del | |
| NM_000515.4:c.292-36del (GH1) | NP_000506.2:n.292-36del | |
| NM_022559.3:c.247-36del (GH1) | NP_072053.1:n.247-36del | |
| NM_022560.3:c.172-36del (GH1) | NP_072054.1:n.172-36del | |
| XM_011524612.1:c.292-36del (GH1) | XP_011522914.1:n.292-36del | |
| NM_000515.5:c.292-36del (GH1) MANE Select | NP_000506.2:n.292-36del | |
| NM_022559.4:c.247-36del (GH1) | NP_072053.1:n.247-36del | |
| NM_022560.4:c.172-36del (GH1) | NP_072054.1:n.172-36del |