Canonical Allele Identifier: CA1677891193

Gene: PRKN

Linked Data

• dbSNP Id: rs4709583
• gnomAD v4: 6-162201272-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162201272A>T , CM000668.2:g.162201272A>T	GRCh38
NC_000006.11:g.162622304A>T , CM000668.1:g.162622304A>T	GRCh37
NC_000006.10:g.162542294A>T	NCBI36
NG_008289.1:g.531531T>A
NG_008289.2:g.531531T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000338468.8:c.412+61253T>A	ENSP00000343589.4:n.412+61253T>A
ENST00000366894.6:c.172-20T>A	ENSP00000355860.2:n.172-20T>A
ENST00000366898.6:c.413-20T>A MANE Select	ENSP00000355865.1:n.413-20T>A
ENST00000673871.1:c.408-20T>A
ENST00000674232.1:n.431-20T>A
ENST00000674436.1:n.49-20T>A
ENST00000674501.1:n.520-20T>A
ENST00000338468.7:c.-40+61253T>A	ENSP00000343589.3:n.-40+61253T>A
ENST00000366892.5:c.413-20T>A	ENSP00000355858.1:n.413-20T>A
ENST00000366894.5:c.-161-20T>A	ENSP00000355860.1:n.-161-20T>A
ENST00000366896.5:c.172-227855T>A	ENSP00000355862.1:n.172-227855T>A
ENST00000366897.5:c.413-20T>A	ENSP00000355863.1:n.413-20T>A
ENST00000366898.5:c.413-20T>A	ENSP00000355865.1:n.413-20T>A
ENST00000479615.5:c.176-20T>A	ENSP00000434414.1:n.176-20T>A
NM_004562.2:c.413-20T>A	NP_004553.2:n.413-20T>A
NM_013987.2:c.413-20T>A	NP_054642.2:n.413-20T>A
NM_013988.2:c.172-227855T>A	NP_054643.2:n.172-227855T>A
XM_011535863.1:c.413-23T>A	XP_011534165.1:n.413-23T>A
XM_011535864.1:c.413-20T>A	XP_011534166.1:n.413-20T>A
XM_011535865.1:c.413-20T>A	XP_011534167.1:n.413-20T>A
XM_011535866.1:c.413-20T>A	XP_011534168.1:n.413-20T>A
XM_011535867.1:c.413-20T>A	XP_011534169.1:n.413-20T>A
XM_017010908.1:c.527-20T>A	XP_016866397.1:n.527-20T>A
XM_017010909.2:c.176-23T>A	XP_016866398.1:n.176-23T>A
XM_024446449.1:c.176-20T>A	XP_024302217.1:n.176-20T>A
XR_001743443.2:n.519-20T>A
NM_004562.3:c.413-20T>A MANE Select	NP_004553.2:n.413-20T>A
NM_013987.3:c.413-20T>A	NP_054642.2:n.413-20T>A
NM_013988.3:c.172-227855T>A	NP_054643.2:n.172-227855T>A