Linked Data
ClinVar Variation Id:
2959537
ClinVar RCV Id:
RCV003811712
gnomAD v4:
17-7220063-AGGGACGGT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7220067_7220074del , CM000679.2:g.7220067_7220074del | GRCh38 |
| NC_000017.10:g.7123386_7123393del , CM000679.1:g.7123386_7123393del | GRCh37 |
| NC_000017.9:g.7064110_7064117del | NCBI36 |
| NG_007975.1:g.5234_5241del | |
| NG_008391.2:g.4980_4987del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.62+21_62+28del MANE Select | ENSP00000349297.5:n.62+21_62+28del | |
| ENST00000322910.9:c.83_90del | ENSP00000325395.5:p.Asp28AlafsTer? | |
| ENST00000350303.9:c.62+21_62+28del | ENSP00000344152.5:n.62+21_62+28del | |
| ENST00000356839.9:c.62+21_62+28del | ENSP00000349297.5:n.62+21_62+28del | |
| ENST00000543245.6:c.132-55_132-48del | ENSP00000438689.2:n.132-55_132-48del | |
| ENST00000577191.5:n.139+21_139+28del | ||
| ENST00000577857.5:n.152+21_152+28del | ||
| ENST00000578269.5:n.169+21_169+28del | ||
| ENST00000578421.1:n.142_149del | ||
| ENST00000579286.5:n.169+21_169+28del | ||
| ENST00000579886.2:c.62+21_62+28del | ENSP00000463246.1:n.62+21_62+28del | |
| ENST00000580263.5:n.152+21_152+28del | ||
| ENST00000581562.5:n.109+21_109+28del | ||
| ENST00000582056.5:n.152+21_152+28del | ||
| ENST00000582356.5:n.187+21_187+28del | ||
| ENST00000583312.5:c.62+21_62+28del | ENSP00000467920.1:n.62+21_62+28del | |
| ENST00000584103.5:c.62+21_62+28del | ENSP00000465353.1:n.62+21_62+28del | |
| NM_000018.3:c.62+21_62+28del | NP_000009.1:n.62+21_62+28del | |
| NM_001033859.2:c.62+21_62+28del | NP_001029031.1:n.62+21_62+28del | |
| NM_001270447.1:c.132-55_132-48del | NP_001257376.1:n.132-55_132-48del | |
| NM_001270448.1:c.-221_-214del | NP_001257377.1:n.-221_-214del | |
| XM_006721516.2:c.62+21_62+28del | XP_006721579.2:n.62+21_62+28del | |
| XM_011523829.1:c.62+21_62+28del | XP_011522131.1:n.62+21_62+28del | |
| XM_011523830.1:c.62+21_62+28del | XP_011522132.1:n.62+21_62+28del | |
| XR_934021.1:n.169+21_169+28del | ||
| XR_934022.1:n.169+21_169+28del | ||
| XR_934023.1:n.169+21_169+28del | ||
| XM_006721516.3:c.62+21_62+28del | XP_006721579.2:n.62+21_62+28del | |
| XM_011523829.2:c.62+21_62+28del | XP_011522131.1:n.62+21_62+28del | |
| XM_011523830.2:c.62+21_62+28del | XP_011522132.1:n.62+21_62+28del | |
| XM_024450741.1:c.62+21_62+28del | XP_024306509.1:n.62+21_62+28del | |
| XR_934021.2:n.121+21_121+28del | ||
| XR_934022.2:n.121+21_121+28del | ||
| XR_934023.2:n.121+21_121+28del | ||
| NM_000018.4:c.62+21_62+28del MANE Select | NP_000009.1:n.62+21_62+28del | |
| NM_001033859.3:c.62+21_62+28del | NP_001029031.1:n.62+21_62+28del | |
| NM_001270447.2:c.132-55_132-48del | NP_001257376.1:n.132-55_132-48del | |
| NM_001270448.2:c.-221_-214del | NP_001257377.1:n.-221_-214del |