Linked Data
dbSNP Id:
rs1555624422
ExAC:
17:74536334 G / GC
gnomAD v2:
17-74536334-G-GC
gnomAD v3:
17-76540252-G-GC
gnomAD v4:
17-76540252-G-GC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.76540252_76540253insC , CM000679.2:g.76540252_76540253insC | GRCh38 |
| NC_000017.10:g.74536334_74536335insC , CM000679.1:g.74536334_74536335insC | GRCh37 |
| NC_000017.9:g.72047929_72047930insC | NCBI36 |
| NG_016702.1:g.17667_17668insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592014.6:c.74+37_74+38insC (PRCD) MANE Select | ENSP00000467661.1:n.74+37_74+38insC | |
| ENST00000397633.7:n.46-253_46-252insC (PRCD) | ||
| ENST00000465808.7:n.93-253_93-252insC (PRCD) | ||
| ENST00000586148.1:c.74+37_74+38insC (PRCD) | ENSP00000465932.1:n.74+37_74+38insC | |
| ENST00000589145.1:c.-52-8562_-52-8561insG (CYGB) | ENSP00000468559.1:n.-52-8562_-52-8561insG | |
| ENST00000590555.5:n.445-253_445-252insC (PRCD) | ||
| ENST00000592014.5:c.74+37_74+38insC (PRCD) | ENSP00000467661.1:n.74+37_74+38insC | |
| ENST00000592432.5:n.249-253_249-252insC (PRCD) | ||
| NM_001077620.2:c.74+37_74+38insC (PRCD) | NP_001071088.1:n.74+37_74+38insC | |
| NR_033357.1:n.249-253_249-252insC (PRCD) | ||
| XM_011524272.1:c.-52-8562_-52-8561insG (CYGB) | XP_011522574.1:n.-52-8562_-52-8561insG | |
| XM_011525184.1:c.197+37_197+38insC (PRCD) | XP_011523486.1:n.197+37_197+38insC | |
| XM_017024116.1:c.-52-8562_-52-8561insG (CYGB) | XP_016879605.1:n.-52-8562_-52-8561insG | |
| XM_017025013.1:c.74+37_74+38insC (PRCD) | XP_016880502.1:n.74+37_74+38insC | |
| XM_017025014.1:c.74+37_74+38insC (PRCD) | XP_016880503.1:n.74+37_74+38insC | |
| XM_017025015.1:c.74+37_74+38insC (PRCD) | XP_016880504.1:n.74+37_74+38insC | |
| NM_001077620.3:c.74+37_74+38insC (PRCD) MANE Select | NP_001071088.1:n.74+37_74+38insC | |
| NR_033357.2:n.249-253_249-252insC (PRCD) |