Linked Data
ClinVar Variation Id:
356021
ClinVar RCV Id:
RCV000280046
dbSNP Id:
rs749081702
ExAC:
6:163148690 G / A
gnomAD v2:
6-163148690-G-A
gnomAD v3:
6-162727658-G-A
gnomAD v4:
6-162727658-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.162727658G>A , CM000668.2:g.162727658G>A | GRCh38 |
| NC_000006.11:g.163148690G>A , CM000668.1:g.163148690G>A | GRCh37 |
| NC_000006.10:g.163068680G>A | NCBI36 |
| NG_008289.1:g.5145C>T | |
| NG_011525.1:g.5527G>A | |
| NG_008289.2:g.5145C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338468.8:c.7+4C>T (PRKN) | ENSP00000343589.4:n.7+4C>T | |
| ENST00000366894.6:c.7+4C>T (PRKN) | ENSP00000355860.2:n.7+4C>T | |
| ENST00000366898.6:c.7+4C>T (PRKN) MANE Select | ENSP00000355865.1:n.7+4C>T | |
| ENST00000642604.1:n.25+4C>T (PRKN) | ||
| ENST00000647006.2:c.-214+4C>T (PRKN) | ENSP00000501337.1:n.-214+4C>T | |
| ENST00000674176.1:n.25+4C>T (PRKN) | ||
| ENST00000674224.1:n.25+4C>T (PRKN) | ||
| ENST00000674232.1:n.25+4C>T (PRKN) | ||
| ENST00000674250.1:c.7+4C>T (PRKN) | ENSP00000501354.1:n.7+4C>T | |
| ENST00000674353.1:n.24+4C>T (PRKN) | ||
| ENST00000674395.1:n.25+4C>T (PRKN) | ||
| ENST00000674493.1:n.24+4C>T (PRKN) | ||
| ENST00000674501.1:n.114+4C>T (PRKN) | ||
| ENST00000337019.7:c.-77+379G>A (PACRG) | ENSP00000337946.3:n.-77+379G>A | |
| ENST00000338468.7:c.-445+4C>T (PRKN) | ENSP00000343589.3:n.-445+4C>T | |
| ENST00000366889.6:c.-77+379G>A (PACRG) | ENSP00000355855.2:n.-77+379G>A | |
| ENST00000366892.5:c.7+4C>T (PRKN) | ENSP00000355858.1:n.7+4C>T | |
| ENST00000366894.5:c.-326+4C>T (PRKN) | ENSP00000355860.1:n.-326+4C>T | |
| ENST00000366896.5:c.7+4C>T (PRKN) | ENSP00000355862.1:n.7+4C>T | |
| ENST00000366897.5:c.7+4C>T (PRKN) | ENSP00000355863.1:n.7+4C>T | |
| ENST00000366898.5:c.7+4C>T (PRKN) | ENSP00000355865.1:n.7+4C>T | |
| ENST00000479615.5:c.-67+4C>T (PRKN) | ENSP00000434414.1:n.-67+4C>T | |
| NM_001080378.1:c.-77+379G>A (PACRG) | NP_001073847.1:n.-77+379G>A | |
| NM_004562.2:c.7+4C>T (PRKN) | NP_004553.2:n.7+4C>T | |
| NM_013987.2:c.7+4C>T (PRKN) | NP_054642.2:n.7+4C>T | |
| NM_013988.2:c.7+4C>T (PRKN) | NP_054643.2:n.7+4C>T | |
| NM_152410.2:c.-77+379G>A (PACRG) | NP_689623.2:n.-77+379G>A | |
| XM_011535456.1:c.-77+379G>A (PACRG) | XP_011533758.1:n.-77+379G>A | |
| XM_011535458.1:c.-77+366G>A (PACRG) | XP_011533760.1:n.-77+366G>A | |
| XM_011535459.1:c.-96G>A (PACRG) | XP_011533761.1:n.-96G>A | |
| XM_011535460.1:c.-77+9G>A (PACRG) | XP_011533762.1:n.-77+9G>A | |
| XM_011535863.1:c.7+4C>T (PRKN) | XP_011534165.1:n.7+4C>T | |
| XM_011535864.1:c.7+4C>T (PRKN) | XP_011534166.1:n.7+4C>T | |
| XM_011535865.1:c.7+4C>T (PRKN) | XP_011534167.1:n.7+4C>T | |
| XM_011535866.1:c.7+4C>T (PRKN) | XP_011534168.1:n.7+4C>T | |
| XM_011535867.1:c.7+4C>T (PRKN) | XP_011534169.1:n.7+4C>T | |
| XM_017010275.2:c.-77+379G>A (PACRG) | XP_016865764.1:n.-77+379G>A | |
| XM_017010277.2:c.-77+366G>A (PACRG) | XP_016865766.1:n.-77+366G>A | |
| XM_017010278.2:c.-96G>A (PACRG) | XP_016865767.1:n.-96G>A | |
| XM_017010279.2:c.-77+9G>A (PACRG) | XP_016865768.1:n.-77+9G>A | |
| XM_017010909.2:c.-67+4C>T (PRKN) | XP_016866398.1:n.-67+4C>T | |
| XM_024446449.1:c.-67+4C>T (PRKN) | XP_024302217.1:n.-67+4C>T | |
| XR_001743443.2:n.113+4C>T (PRKN) | ||
| NM_004562.3:c.7+4C>T (PRKN) MANE Select | NP_004553.2:n.7+4C>T | |
| NM_013987.3:c.7+4C>T (PRKN) | NP_054642.2:n.7+4C>T | |
| NM_013988.3:c.7+4C>T (PRKN) | NP_054643.2:n.7+4C>T | |
| NM_001080378.2:c.-77+379G>A (PACRG) | NP_001073847.1:n.-77+379G>A | |
| NM_152410.3:c.-77+379G>A (PACRG) | NP_689623.2:n.-77+379G>A |