Canonical Allele Identifier: CA4090532
Gene: PRKN HGNC NCBI

Linked Data

dbSNP Id: rs748110477

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.162443458T>C , CM000668.2:g.162443458T>C GRCh38
NC_000006.11:g.162864490T>C , CM000668.1:g.162864490T>C GRCh37
NC_000006.10:g.162784480T>C NCBI36
NG_008289.1:g.289345A>G
NG_008289.2:g.289345A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338468.8:c.23A>G ENSP00000343589.4:p.Asn8Ser
ENST00000366894.6:c.23A>G ENSP00000355860.2:p.Asn8Ser
ENST00000366898.6:c.23A>G MANE Select ENSP00000355865.1:p.Asn8Ser
ENST00000648830.1:n.190A>G
ENST00000673871.1:c.18A>G
ENST00000674232.1:n.41A>G
ENST00000674259.1:n.80A>G
ENST00000674493.1:n.40A>G
ENST00000674501.1:n.130A>G
ENST00000338468.7:c.-429A>G ENSP00000343589.3:n.-429A>G
ENST00000366892.5:c.23A>G ENSP00000355858.1:p.Asn8Ser
ENST00000366894.5:c.-310A>G ENSP00000355860.1:n.-310A>G
ENST00000366896.5:c.23A>G ENSP00000355862.1:p.Asn8Ser
ENST00000366897.5:c.23A>G ENSP00000355863.1:p.Asn8Ser
ENST00000366898.5:c.23A>G ENSP00000355865.1:p.Asn8Ser
ENST00000479615.5:c.-66-180693A>G ENSP00000434414.1:n.-66-180693A>G
NM_004562.2:c.23A>G NP_004553.2:p.Asn8Ser
NM_013987.2:c.23A>G NP_054642.2:p.Asn8Ser
NM_013988.2:c.23A>G NP_054643.2:p.Asn8Ser
XM_011535863.1:c.23A>G XP_011534165.1:p.Asn8Ser
XM_011535864.1:c.23A>G XP_011534166.1:p.Asn8Ser
XM_011535865.1:c.23A>G XP_011534167.1:p.Asn8Ser
XM_011535866.1:c.23A>G XP_011534168.1:p.Asn8Ser
XM_011535867.1:c.23A>G XP_011534169.1:p.Asn8Ser
XM_017010908.1:c.137A>G XP_016866397.1:p.Asn46Ser
XM_017010909.2:c.-66-180693A>G XP_016866398.1:n.-66-180693A>G
XM_024446449.1:c.-66-180693A>G XP_024302217.1:n.-66-180693A>G
XR_001743443.2:n.129A>G
NM_004562.3:c.23A>G MANE Select NP_004553.2:p.Asn8Ser
NM_013987.3:c.23A>G NP_054642.2:p.Asn8Ser
NM_013988.3:c.23A>G NP_054643.2:p.Asn8Ser