Canonical Allele Identifier: CA453189934

Gene: PRKN

Linked Data

• MyVariant Identifiers: chr6:g.162864372C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443340C>T , CM000668.2:g.162443340C>T	GRCh38
NC_000006.11:g.162864372C>T , CM000668.1:g.162864372C>T	GRCh37
NC_000006.10:g.162784362C>T	NCBI36
NG_008289.1:g.289463G>A
NG_008289.2:g.289463G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.141G>A	ENSP00000343589.4:p.Gly47=
ENST00000366894.6:c.141G>A	ENSP00000355860.2:p.Gly47=
ENST00000366898.6:c.141G>A MANE Select	ENSP00000355865.1:p.Gly47=
ENST00000648830.1:n.308G>A
ENST00000673871.1:c.136G>A
ENST00000674232.1:n.159G>A
ENST00000674259.1:n.198G>A
ENST00000674493.1:n.158G>A
ENST00000674501.1:n.248G>A
ENST00000338468.7:c.-311G>A	ENSP00000343589.3:n.-311G>A
ENST00000366892.5:c.141G>A	ENSP00000355858.1:p.Gly47=
ENST00000366894.5:c.-192G>A	ENSP00000355860.1:n.-192G>A
ENST00000366896.5:c.141G>A	ENSP00000355862.1:p.Gly47=
ENST00000366897.5:c.141G>A	ENSP00000355863.1:p.Gly47=
ENST00000366898.5:c.141G>A	ENSP00000355865.1:p.Gly47=
ENST00000479615.5:c.-66-180575G>A	ENSP00000434414.1:n.-66-180575G>A
NM_004562.2:c.141G>A	NP_004553.2:p.Gly47=
NM_013987.2:c.141G>A	NP_054642.2:p.Gly47=
NM_013988.2:c.141G>A	NP_054643.2:p.Gly47=
XM_011535863.1:c.141G>A	XP_011534165.1:p.Gly47=
XM_011535864.1:c.141G>A	XP_011534166.1:p.Gly47=
XM_011535865.1:c.141G>A	XP_011534167.1:p.Gly47=
XM_011535866.1:c.141G>A	XP_011534168.1:p.Gly47=
XM_011535867.1:c.141G>A	XP_011534169.1:p.Gly47=
XM_017010908.1:c.255G>A	XP_016866397.1:p.Gly85=
XM_017010909.2:c.-66-180575G>A	XP_016866398.1:n.-66-180575G>A
XM_024446449.1:c.-66-180575G>A	XP_024302217.1:n.-66-180575G>A
XR_001743443.2:n.247G>A
NM_004562.3:c.141G>A MANE Select	NP_004553.2:p.Gly47=
NM_013987.3:c.141G>A	NP_054642.2:p.Gly47=
NM_013988.3:c.141G>A	NP_054643.2:p.Gly47=