Linked Data
ClinVar Variation Id:
51088
ClinVar RCV Id:
RCV002267808
dbSNP Id:
rs80359270
gnomAD v4:
13-32332710-T-TA
PubMed:
PMID:20104584
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32332711dup , CM000675.2:g.32332711dup | GRCh38 |
| NC_000013.10:g.32906848dup , CM000675.1:g.32906848dup | GRCh37 |
| NC_000013.9:g.31804848dup | NCBI36 |
| NG_012772.3:g.22232dup , LRG_293:g.22232dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000470094.2:c.1233dup | ENSP00000434898.2:p.Pro412ThrfsTer9 | |
| ENST00000528762.2:c.1233dup | ENSP00000433168.2:p.Pro412ThrfsTer9 | |
| ENST00000530893.7:c.864dup | ENSP00000499438.2:p.Pro289ThrfsTer9 | |
| ENST00000665585.2:c.1233dup | ENSP00000499570.2:p.Pro412ThrfsTer9 | |
| ENST00000666593.2:c.1233dup | ENSP00000499256.2:p.Pro412ThrfsTer9 | |
| ENST00000700202.2:c.1233dup | ENSP00000514856.2:p.Pro412ThrfsTer9 | |
| ENST00000700201.1:c.*1012dup | ENSP00000514855.1:n.*1012dup | |
| ENST00000380152.8:c.1233dup MANE Select | ENSP00000369497.3:p.Pro412ThrfsTer9 | |
| ENST00000544455.6:c.1233dup | ENSP00000439902.1:p.Pro412ThrfsTer9 | |
| ENST00000614259.2:c.1233dup | ENSP00000506251.1:p.Pro412ThrfsTer9 | |
| ENST00000680887.1:c.1233dup | ENSP00000505508.1:p.Pro412ThrfsTer9 | |
| ENST00000380152.7:c.1233dup | ENSP00000369497.3:p.Pro412ThrfsTer9 | |
| ENST00000530893.6:n.1431dup | ||
| ENST00000544455.5:c.1233dup | ENSP00000439902.1:p.Pro412ThrfsTer9 | |
| ENST00000614259.1:n.1233dup | ||
| NM_000059.3:c.1233dup , LRG_293t1:c.1233dup | NP_000050.2:p.Pro412ThrfsTer9 | |
| XM_011535203.1:c.1233dup | XP_011533505.1:p.Pro412ThrfsTer9 | |
| XM_011535204.1:c.1233dup | XP_011533506.1:p.Pro412ThrfsTer9 | |
| XM_011535205.1:c.1233dup | XP_011533507.1:p.Pro412ThrfsTer9 | |
| NM_000059.4:c.1233dup MANE Select | NP_000050.3:p.Pro412ThrfsTer9 |