Canonical Allele Identifier: CA366477388

Gene: PRKN

Linked Data

• ClinVar Variation Id: 662122
• ClinVar RCV Id: RCV000819694
• dbSNP Id: rs199859147
• MyVariant Identifiers: chr6:g.162864445A>T (hg19) ; chr6:g.162443413A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443413A>T , CM000668.2:g.162443413A>T	GRCh38
NC_000006.11:g.162864445A>T , CM000668.1:g.162864445A>T	GRCh37
NC_000006.10:g.162784435A>T	NCBI36
NG_008289.1:g.289390T>A
NG_008289.2:g.289390T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.68T>A	ENSP00000343589.4:p.Ile23Asn
ENST00000366894.6:c.68T>A	ENSP00000355860.2:p.Ile23Asn
ENST00000366898.6:c.68T>A MANE Select	ENSP00000355865.1:p.Ile23Asn
ENST00000648830.1:n.235T>A
ENST00000673871.1:c.63T>A
ENST00000674232.1:n.86T>A
ENST00000674259.1:n.125T>A
ENST00000674493.1:n.85T>A
ENST00000674501.1:n.175T>A
ENST00000338468.7:c.-384T>A	ENSP00000343589.3:n.-384T>A
ENST00000366892.5:c.68T>A	ENSP00000355858.1:p.Ile23Asn
ENST00000366894.5:c.-265T>A	ENSP00000355860.1:n.-265T>A
ENST00000366896.5:c.68T>A	ENSP00000355862.1:p.Ile23Asn
ENST00000366897.5:c.68T>A	ENSP00000355863.1:p.Ile23Asn
ENST00000366898.5:c.68T>A	ENSP00000355865.1:p.Ile23Asn
ENST00000479615.5:c.-66-180648T>A	ENSP00000434414.1:n.-66-180648T>A
NM_004562.2:c.68T>A	NP_004553.2:p.Ile23Asn
NM_013987.2:c.68T>A	NP_054642.2:p.Ile23Asn
NM_013988.2:c.68T>A	NP_054643.2:p.Ile23Asn
XM_011535863.1:c.68T>A	XP_011534165.1:p.Ile23Asn
XM_011535864.1:c.68T>A	XP_011534166.1:p.Ile23Asn
XM_011535865.1:c.68T>A	XP_011534167.1:p.Ile23Asn
XM_011535866.1:c.68T>A	XP_011534168.1:p.Ile23Asn
XM_011535867.1:c.68T>A	XP_011534169.1:p.Ile23Asn
XM_017010908.1:c.182T>A	XP_016866397.1:p.Ile61Asn
XM_017010909.2:c.-66-180648T>A	XP_016866398.1:n.-66-180648T>A
XM_024446449.1:c.-66-180648T>A	XP_024302217.1:n.-66-180648T>A
XR_001743443.2:n.174T>A
NM_004562.3:c.68T>A MANE Select	NP_004553.2:p.Ile23Asn
NM_013987.3:c.68T>A	NP_054642.2:p.Ile23Asn
NM_013988.3:c.68T>A	NP_054643.2:p.Ile23Asn