MyVariant.info:
GRCh37
chr10:g.53059406T>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.51299646T>G , CM000672.2:g.51299646T>G | GRCh38 |
| NC_000010.10:g.53059406T>G , CM000672.1:g.53059406T>G | GRCh37 |
| NC_000010.9:g.52729412T>G | NCBI36 |
| NG_029982.1:g.313496T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373976.9:c.478+146316T>G (PRKG1) | ENSP00000363087.4:n.478+146316T>G | |
| ENST00000373980.11:c.478+146316T>G (PRKG1) MANE Select | ENSP00000363092.5:n.478+146316T>G | |
| ENST00000401604.8:c.433+146316T>G (PRKG1) | ENSP00000384200.4:n.433+146316T>G | |
| ENST00000643582.1:c.478+146316T>G (PRKG1) | ENSP00000495279.1:n.478+146316T>G | |
| ENST00000643704.1:c.478+146316T>G (PRKG1) | ENSP00000496551.1:n.478+146316T>G | |
| ENST00000645324.1:c.478+146316T>G (PRKG1) | ENSP00000494124.1:n.478+146316T>G | |
| ENST00000373976.8:c.52+146316T>G (PRKG1) | ENSP00000363087.3:n.52+146316T>G | |
| ENST00000373980.8:c.478+146316T>G (PRKG1) | ENSP00000363092.4:n.478+146316T>G | |
| ENST00000373985.5:c.433+146316T>G (PRKG1) | ENSP00000363097.2:n.433+146316T>G | |
| NM_001098512.2:c.433+146316T>G (PRKG1) | NP_001091982.1:n.433+146316T>G | |
| NM_006258.3:c.478+146316T>G (PRKG1) | NP_006249.1:n.478+146316T>G | |
| NR_030336.1:n.74T>G (MIR605) | ||
| XM_011539952.1:c.478+146316T>G (PRKG1) | XP_011538254.1:n.478+146316T>G | |
| NM_001098512.3:c.433+146316T>G (PRKG1) | NP_001091982.1:n.433+146316T>G | |
| NM_006258.4:c.478+146316T>G (PRKG1) MANE Select | NP_006249.1:n.478+146316T>G | |
| XM_011539952.2:c.478+146316T>G (PRKG1) | XP_011538254.1:n.478+146316T>G | |
| XM_017016412.1:c.193+146316T>G (PRKG1) | XP_016871901.1:n.193+146316T>G | |
| XM_017016413.1:c.175+146316T>G (PRKG1) | XP_016871902.1:n.175+146316T>G | |
| NM_001374782.1:c.478+146316T>G (PRKG1) | NP_001361711.1:n.478+146316T>G |