Linked Data
dbSNP Id:
rs773995352
gnomAD v2:
17-74536337-G-GT
gnomAD v4:
17-76540255-G-GT
MyVariant Identifiers:
chr17:g.74536337_74536338insT (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.76540255_76540256insT , CM000679.2:g.76540255_76540256insT | GRCh38 |
| NC_000017.10:g.74536337_74536338insT , CM000679.1:g.74536337_74536338insT | GRCh37 |
| NC_000017.9:g.72047932_72047933insT | NCBI36 |
| NG_016702.1:g.17670_17671insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592014.6:c.74+40_74+41insT (PRCD) MANE Select | ENSP00000467661.1:n.74+40_74+41insT | |
| ENST00000397633.7:n.46-250_46-249insT (PRCD) | ||
| ENST00000465808.7:n.93-250_93-249insT (PRCD) | ||
| ENST00000586148.1:c.74+40_74+41insT (PRCD) | ENSP00000465932.1:n.74+40_74+41insT | |
| ENST00000589145.1:c.-52-8565_-52-8564insA (CYGB) | ENSP00000468559.1:n.-52-8565_-52-8564insA | |
| ENST00000590555.5:n.445-250_445-249insT (PRCD) | ||
| ENST00000592014.5:c.74+40_74+41insT (PRCD) | ENSP00000467661.1:n.74+40_74+41insT | |
| ENST00000592432.5:n.249-250_249-249insT (PRCD) | ||
| NM_001077620.2:c.74+40_74+41insT (PRCD) | NP_001071088.1:n.74+40_74+41insT | |
| NR_033357.1:n.249-250_249-249insT (PRCD) | ||
| XM_011524272.1:c.-52-8565_-52-8564insA (CYGB) | XP_011522574.1:n.-52-8565_-52-8564insA | |
| XM_011525184.1:c.197+40_197+41insT (PRCD) | XP_011523486.1:n.197+40_197+41insT | |
| XM_017024116.1:c.-52-8565_-52-8564insA (CYGB) | XP_016879605.1:n.-52-8565_-52-8564insA | |
| XM_017025013.1:c.74+40_74+41insT (PRCD) | XP_016880502.1:n.74+40_74+41insT | |
| XM_017025014.1:c.74+40_74+41insT (PRCD) | XP_016880503.1:n.74+40_74+41insT | |
| XM_017025015.1:c.74+40_74+41insT (PRCD) | XP_016880504.1:n.74+40_74+41insT | |
| NM_001077620.3:c.74+40_74+41insT (PRCD) MANE Select | NP_001071088.1:n.74+40_74+41insT | |
| NR_033357.2:n.249-250_249-249insT (PRCD) |