Canonical Allele Identifier: CA1677459155

Gene: PRKN

Linked Data

• dbSNP Id: rs1784456363
• gnomAD v4: 6-161350027-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161350027G>A , CM000668.2:g.161350027G>A	GRCh38
NC_000006.11:g.161771059G>A , CM000668.1:g.161771059G>A	GRCh37
NC_000006.10:g.161691049G>A	NCBI36
NG_008289.1:g.1382776C>T
NG_008289.2:g.1382776C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366898.6:c.*72C>T MANE Select	ENSP00000355865.1:n.*72C>T
ENST00000673871.1:c.1551C>T
ENST00000674006.1:n.855C>T
ENST00000674436.1:n.1106C>T
ENST00000366896.5:c.*72C>T	ENSP00000355862.1:n.*72C>T
ENST00000366897.5:c.*72C>T	ENSP00000355863.1:n.*72C>T
ENST00000366898.5:c.*72C>T	ENSP00000355865.1:n.*72C>T
NM_004562.2:c.*72C>T	NP_004553.2:n.*72C>T
NM_013987.2:c.*72C>T	NP_054642.2:n.*72C>T
NM_013988.2:c.*72C>T	NP_054643.2:n.*72C>T
XM_011535863.1:c.*72C>T	XP_011534165.1:n.*72C>T
XM_017010908.1:c.*72C>T	XP_016866397.1:n.*72C>T
XM_017010909.2:c.*72C>T	XP_016866398.1:n.*72C>T
XM_024446449.1:c.*72C>T	XP_024302217.1:n.*72C>T
XR_001743443.2:n.1662C>T
NM_004562.3:c.*72C>T MANE Select	NP_004553.2:n.*72C>T
NM_013987.3:c.*72C>T	NP_054642.2:n.*72C>T
NM_013988.3:c.*72C>T	NP_054643.2:n.*72C>T