Linked Data
ClinVar Variation Id:
502532
ClinVar RCV Id:
RCV000592303
dbSNP Id:
rs1452573962
gnomAD v2:
9-71820181-TC-T
gnomAD v3:
9-69205265-TC-T
gnomAD v4:
9-69205265-TC-T
MyVariant Identifiers:
chr9:g.71820185del (hg19)
chr9:g.71820182del (hg19)
chr9:g.69205269del (hg38)
chr9:g.69205266del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.69205269del , CM000671.2:g.69205269del | GRCh38 |
| NC_000009.11:g.71820185del , CM000671.1:g.71820185del | GRCh37 |
| NC_000009.10:g.71010005del | NCBI36 |
| NG_016342.1:g.88962del | |
| NG_016342.2:g.109363del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000348208.9:c.61-7279del | ENSP00000345893.4:n.61-7279del | |
| ENST00000377245.9:c.61-7279del MANE Select | ENSP00000366453.4:n.61-7279del | |
| ENST00000423935.6:c.-9-7279del | ENSP00000402941.1:n.-9-7279del | |
| ENST00000535702.6:c.72+36del | ENSP00000442090.1:n.72+36del | |
| ENST00000539225.2:c.108del | ENSP00000438262.1:p.Asn37ThrfsTer22 | |
| ENST00000636247.1:n.140-7279del | ||
| ENST00000636438.1:c.238-7279del | ENSP00000489860.1:n.238-7279del | |
| ENST00000642889.1:c.448-7279del | ENSP00000493780.1:n.448-7279del | |
| ENST00000643352.1:c.*249-7279del | ENSP00000496488.1:n.*249-7279del | |
| ENST00000643713.1:c.-9-7279del | ENSP00000494704.1:n.-9-7279del | |
| ENST00000643765.1:c.763-7279del | ||
| ENST00000645088.1:c.*368-7279del | ENSP00000495447.1:n.*368-7279del | |
| ENST00000646862.1:c.667-7279del | ENSP00000494599.1:n.667-7279del | |
| ENST00000647986.1:c.-9-7279del | ENSP00000496877.1:n.-9-7279del | |
| ENST00000648087.1:n.378-7279del | ||
| ENST00000648402.1:c.-1002del | ENSP00000497596.1:n.-1002del | |
| ENST00000649114.1:c.61-7279del | ENSP00000497328.1:n.61-7279del | |
| ENST00000649134.1:c.72+36del | ENSP00000498068.1:n.72+36del | |
| ENST00000649783.1:n.84+36del | ||
| ENST00000649939.1:c.-10+160del | ENSP00000498043.1:n.-10+160del | |
| ENST00000649943.1:c.61-7279del | ENSP00000497539.1:n.61-7279del | |
| ENST00000650084.1:c.63+36del | ENSP00000497861.1:n.63+36del | |
| ENST00000650333.1:c.-9-7279del | ENSP00000496791.1:n.-9-7279del | |
| ENST00000650522.1:n.84+36del | ||
| ENST00000265384.11:c.61-7279del | ENSP00000265384.7:n.61-7279del | |
| ENST00000348208.8:c.61-7279del | ENSP00000345893.4:n.61-7279del | |
| ENST00000377245.8:c.61-7279del | ENSP00000366453.4:n.61-7279del | |
| ENST00000377259.5:c.-9-7279del | ENSP00000366469.1:n.-9-7279del | |
| ENST00000423935.5:c.-9-7279del | ENSP00000402941.1:n.-9-7279del | |
| ENST00000453658.6:c.-9-7279del | ENSP00000392178.2:n.-9-7279del | |
| ENST00000535702.5:c.72+36del | ENSP00000442090.1:n.72+36del | |
| ENST00000539225.1:c.108del | ENSP00000438262.1:p.Asn37ThrfsTer22 | |
| ENST00000606364.5:c.-9-7279del | ENSP00000475926.1:n.-9-7279del | |
| NM_001170414.2:c.-9-7279del | NP_001163885.1:n.-9-7279del | |
| NM_001170415.1:c.72+36del | NP_001163886.1:n.72+36del | |
| NM_001170416.1:c.108del | NP_001163887.1:p.Asn37ThrfsTer22 | |
| NM_001170630.1:c.61-7279del | NP_001164101.1:n.61-7279del | |
| NM_004817.3:c.61-7279del | NP_004808.2:n.61-7279del | |
| NM_201629.3:c.61-7279del | NP_963923.1:n.61-7279del | |
| XM_005252314.1:c.72+36del | XP_005252371.1:n.72+36del | |
| XM_006717324.2:c.55-7279del | XP_006717387.1:n.55-7279del | |
| XM_011519204.1:c.-9-7279del | XP_011517506.1:n.-9-7279del | |
| XM_011519205.1:c.-9-7279del | XP_011517507.1:n.-9-7279del | |
| XM_011519206.1:c.-9-7279del | XP_011517508.1:n.-9-7279del | |
| XM_011519207.1:c.-9-7279del | XP_011517509.1:n.-9-7279del | |
| XM_011519208.1:c.-9-7279del | XP_011517510.1:n.-9-7279del | |
| XM_011519209.1:c.-9-7279del | XP_011517511.1:n.-9-7279del | |
| NM_004817.4:c.61-7279del MANE Select | NP_004808.2:n.61-7279del | |
| XM_005252314.2:c.72+36del | XP_005252371.1:n.72+36del | |
| XM_011519206.2:c.-9-7279del | XP_011517508.1:n.-9-7279del | |
| XM_011519207.2:c.-9-7279del | XP_011517509.1:n.-9-7279del | |
| XM_011519208.2:c.-9-7279del | XP_011517510.1:n.-9-7279del | |
| XM_011519209.2:c.-9-7279del | XP_011517511.1:n.-9-7279del | |
| XM_017015327.2:c.61-7279del | XP_016870816.1:n.61-7279del | |
| XM_017015328.1:c.72+36del | XP_016870817.1:n.72+36del | |
| NM_001170416.2:c.108del | NP_001163887.1:p.Asn37ThrfsTer22 | |
| NM_001369870.1:c.-9-7279del | NP_001356799.1:n.-9-7279del | |
| NM_001369871.1:c.-9-7279del | NP_001356800.1:n.-9-7279del | |
| NM_001369872.1:c.61-7279del | NP_001356801.1:n.61-7279del | |
| NM_001369873.1:c.61-7279del | NP_001356802.1:n.61-7279del | |
| NM_001369874.1:c.72+36del | NP_001356803.1:n.72+36del | |
| NM_001369875.1:c.72+36del | NP_001356804.1:n.72+36del |