Canonical Allele Identifier: CA2681114239

Gene: PRKN

Linked Data

• gnomAD v4: 6-161785959-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161785959G>T , CM000668.2:g.161785959G>T	GRCh38
NC_000006.11:g.162206991G>T , CM000668.1:g.162206991G>T	GRCh37
NC_000006.10:g.162126981G>T	NCBI36
NG_008289.1:g.946844C>A
NG_008289.2:g.946844C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.613-51C>A	ENSP00000343589.4:n.613-51C>A
ENST00000366894.6:c.494-51C>A	ENSP00000355860.2:n.494-51C>A
ENST00000366898.6:c.735-51C>A MANE Select	ENSP00000355865.1:n.735-51C>A
ENST00000673871.1:c.730-51C>A
ENST00000674006.1:n.120-51C>A
ENST00000674436.1:n.371-51C>A
ENST00000674501.1:n.842-51C>A
ENST00000338468.7:c.162-51C>A	ENSP00000343589.3:n.162-51C>A
ENST00000366892.5:c.735-51C>A	ENSP00000355858.1:n.735-51C>A
ENST00000366894.5:c.162-51C>A	ENSP00000355860.1:n.162-51C>A
ENST00000366896.5:c.288-51C>A	ENSP00000355862.1:n.288-51C>A
ENST00000366897.5:c.651-51C>A	ENSP00000355863.1:n.651-51C>A
ENST00000366898.5:c.735-51C>A	ENSP00000355865.1:n.735-51C>A
ENST00000479615.5:c.498-51C>A	ENSP00000434414.1:n.498-51C>A
NM_004562.2:c.735-51C>A	NP_004553.2:n.735-51C>A
NM_013987.2:c.651-51C>A	NP_054642.2:n.651-51C>A
NM_013988.2:c.288-51C>A	NP_054643.2:n.288-51C>A
XM_011535863.1:c.732-51C>A	XP_011534165.1:n.732-51C>A
XM_011535864.1:c.735-51C>A	XP_011534166.1:n.735-51C>A
XM_011535865.1:c.735-51C>A	XP_011534167.1:n.735-51C>A
XM_017010908.1:c.849-51C>A	XP_016866397.1:n.849-51C>A
XM_017010909.2:c.495-51C>A	XP_016866398.1:n.495-51C>A
XM_024446449.1:c.498-51C>A	XP_024302217.1:n.498-51C>A
XR_001743443.2:n.841-51C>A
NM_004562.3:c.735-51C>A MANE Select	NP_004553.2:n.735-51C>A
NM_013987.3:c.651-51C>A	NP_054642.2:n.651-51C>A
NM_013988.3:c.288-51C>A	NP_054643.2:n.288-51C>A