Linked Data
ClinVar Variation Id:
37735
dbSNP Id:
rs80359273
ExAC:
13:32906876 CA / C
gnomAD v2:
13-32906876-CA-C
gnomAD v3:
13-32332739-CA-C
gnomAD v4:
13-32332739-CA-C
MyVariant Identifiers:
chr13:g.32906880del (hg19)
chr13:g.32906877del (hg19)
chr13:g.32332743del (hg38)
chr13:g.32332740del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32332743del , CM000675.2:g.32332743del | GRCh38 |
| NC_000013.10:g.32906880del , CM000675.1:g.32906880del | GRCh37 |
| NC_000013.9:g.31804880del | NCBI36 |
| NG_012772.3:g.22264del , LRG_293:g.22264del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000470094.2:c.1265del | ENSP00000434898.2:p.Asn422IlefsTer8 | |
| ENST00000528762.2:c.1265del | ENSP00000433168.2:p.Asn422IlefsTer8 | |
| ENST00000530893.7:c.896del | ENSP00000499438.2:p.Asn299IlefsTer8 | |
| ENST00000665585.2:c.1265del | ENSP00000499570.2:p.Asn422IlefsTer8 | |
| ENST00000666593.2:c.1265del | ENSP00000499256.2:p.Asn422IlefsTer8 | |
| ENST00000700202.2:c.1265del | ENSP00000514856.2:p.Asn422IlefsTer8 | |
| ENST00000700201.1:c.*1044del | ENSP00000514855.1:n.*1044del | |
| ENST00000380152.8:c.1265del MANE Select | ENSP00000369497.3:p.Asn422IlefsTer8 | |
| ENST00000544455.6:c.1265del | ENSP00000439902.1:p.Asn422IlefsTer8 | |
| ENST00000614259.2:c.1265del | ENSP00000506251.1:p.Asn422IlefsTer8 | |
| ENST00000680887.1:c.1265del | ENSP00000505508.1:p.Asn422IlefsTer8 | |
| ENST00000380152.7:c.1265del | ENSP00000369497.3:p.Asn422IlefsTer8 | |
| ENST00000530893.6:n.1463del | ||
| ENST00000544455.5:c.1265del | ENSP00000439902.1:p.Asn422IlefsTer8 | |
| ENST00000614259.1:n.1265del | ||
| NM_000059.3:c.1265del , LRG_293t1:c.1265del | NP_000050.2:p.Asn422IlefsTer8 | |
| XM_011535203.1:c.1265del | XP_011533505.1:p.Asn422IlefsTer8 | |
| XM_011535204.1:c.1265del | XP_011533506.1:p.Asn422IlefsTer8 | |
| XM_011535205.1:c.1265del | XP_011533507.1:p.Asn422IlefsTer8 | |
| NM_000059.4:c.1265del MANE Select | NP_000050.3:p.Asn422IlefsTer8 |