Canonical Allele Identifier: CA2713717612
Gene: PRKN HGNC NCBI

Linked Data

dbSNP Id: rs2128232826

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.161893908C>G , CM000668.2:g.161893908C>G GRCh38
NC_000006.11:g.162314940C>G , CM000668.1:g.162314940C>G GRCh37
NC_000006.10:g.162234930C>G NCBI36
NG_008289.1:g.838895G>C
NG_008289.2:g.838895G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000338468.8:c.612+79394G>C ENSP00000343589.4:n.612+79394G>C
ENST00000366894.6:c.493+79394G>C ENSP00000355860.2:n.493+79394G>C
ENST00000366898.6:c.734+79394G>C MANE Select ENSP00000355865.1:n.734+79394G>C
ENST00000673871.1:c.729+79394G>C
ENST00000674436.1:n.370+79394G>C
ENST00000674501.1:n.841+79394G>C
ENST00000338468.7:c.161+79394G>C ENSP00000343589.3:n.161+79394G>C
ENST00000366892.5:c.734+79394G>C ENSP00000355858.1:n.734+79394G>C
ENST00000366894.5:c.161+79394G>C ENSP00000355860.1:n.161+79394G>C
ENST00000366896.5:c.287+79394G>C ENSP00000355862.1:n.287+79394G>C
ENST00000366897.5:c.650+79394G>C ENSP00000355863.1:n.650+79394G>C
ENST00000366898.5:c.734+79394G>C ENSP00000355865.1:n.734+79394G>C
ENST00000479615.5:c.497+79394G>C ENSP00000434414.1:n.497+79394G>C
NM_004562.2:c.734+79394G>C NP_004553.2:n.734+79394G>C
NM_013987.2:c.650+79394G>C NP_054642.2:n.650+79394G>C
NM_013988.2:c.287+79394G>C NP_054643.2:n.287+79394G>C
XM_011535863.1:c.731+79394G>C XP_011534165.1:n.731+79394G>C
XM_011535864.1:c.734+79394G>C XP_011534166.1:n.734+79394G>C
XM_011535865.1:c.734+79394G>C XP_011534167.1:n.734+79394G>C
XM_017010908.1:c.848+79394G>C XP_016866397.1:n.848+79394G>C
XM_017010909.2:c.494+79394G>C XP_016866398.1:n.494+79394G>C
XM_024446449.1:c.497+79394G>C XP_024302217.1:n.497+79394G>C
XR_001743443.2:n.840+79394G>C
NM_004562.3:c.734+79394G>C MANE Select NP_004553.2:n.734+79394G>C
NM_013987.3:c.650+79394G>C NP_054642.2:n.650+79394G>C
NM_013988.3:c.287+79394G>C NP_054643.2:n.287+79394G>C