Canonical Allele Identifier: CA1677680453

Gene: PRKN

Linked Data

• dbSNP Id: rs1272898370

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161785915A>G , CM000668.2:g.161785915A>G	GRCh38
NC_000006.11:g.162206947A>G , CM000668.1:g.162206947A>G	GRCh37
NC_000006.10:g.162126937A>G	NCBI36
NG_008289.1:g.946888T>C
NG_008289.2:g.946888T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.613-7T>C	ENSP00000343589.4:n.613-7T>C
ENST00000366894.6:c.494-7T>C	ENSP00000355860.2:n.494-7T>C
ENST00000366898.6:c.735-7T>C MANE Select	ENSP00000355865.1:n.735-7T>C
ENST00000673871.1:c.730-7T>C
ENST00000674006.1:n.120-7T>C
ENST00000674436.1:n.371-7T>C
ENST00000674501.1:n.842-7T>C
ENST00000338468.7:c.162-7T>C	ENSP00000343589.3:n.162-7T>C
ENST00000366892.5:c.735-7T>C	ENSP00000355858.1:n.735-7T>C
ENST00000366894.5:c.162-7T>C	ENSP00000355860.1:n.162-7T>C
ENST00000366896.5:c.288-7T>C	ENSP00000355862.1:n.288-7T>C
ENST00000366897.5:c.651-7T>C	ENSP00000355863.1:n.651-7T>C
ENST00000366898.5:c.735-7T>C	ENSP00000355865.1:n.735-7T>C
ENST00000479615.5:c.498-7T>C	ENSP00000434414.1:n.498-7T>C
NM_004562.2:c.735-7T>C	NP_004553.2:n.735-7T>C
NM_013987.2:c.651-7T>C	NP_054642.2:n.651-7T>C
NM_013988.2:c.288-7T>C	NP_054643.2:n.288-7T>C
XM_011535863.1:c.732-7T>C	XP_011534165.1:n.732-7T>C
XM_011535864.1:c.735-7T>C	XP_011534166.1:n.735-7T>C
XM_011535865.1:c.735-7T>C	XP_011534167.1:n.735-7T>C
XM_017010908.1:c.849-7T>C	XP_016866397.1:n.849-7T>C
XM_017010909.2:c.495-7T>C	XP_016866398.1:n.495-7T>C
XM_024446449.1:c.498-7T>C	XP_024302217.1:n.498-7T>C
XR_001743443.2:n.841-7T>C
NM_004562.3:c.735-7T>C MANE Select	NP_004553.2:n.735-7T>C
NM_013987.3:c.651-7T>C	NP_054642.2:n.651-7T>C
NM_013988.3:c.288-7T>C	NP_054643.2:n.288-7T>C