Canonical Allele Identifier: CA1678013002

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443330T= , CM000668.2:g.162443330T=	GRCh38
NC_000006.11:g.162864362T= , CM000668.1:g.162864362T=	GRCh37
NC_000006.10:g.162784352T=	NCBI36
NG_008289.1:g.289473A=
NG_008289.2:g.289473A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.151A=	ENSP00000343589.4:p.Arg51=
ENST00000366894.6:c.151A=	ENSP00000355860.2:p.Arg51=
ENST00000366898.6:c.151A= MANE Select	ENSP00000355865.1:p.Arg51=
ENST00000648830.1:n.318A=
ENST00000673871.1:c.146A=
ENST00000674232.1:n.169A=
ENST00000674259.1:n.208A=
ENST00000674493.1:n.168A=
ENST00000674501.1:n.258A=
ENST00000338468.7:c.-301A=	ENSP00000343589.3:n.-301A=
ENST00000366892.5:c.151A=	ENSP00000355858.1:p.Arg51=
ENST00000366894.5:c.-182A=	ENSP00000355860.1:n.-182A=
ENST00000366896.5:c.151A=	ENSP00000355862.1:p.Arg51=
ENST00000366897.5:c.151A=	ENSP00000355863.1:p.Arg51=
ENST00000366898.5:c.151A=	ENSP00000355865.1:p.Arg51=
ENST00000479615.5:c.-66-180565A=	ENSP00000434414.1:n.-66-180565A=
NM_004562.2:c.151A=	NP_004553.2:p.Arg51=
NM_013987.2:c.151A=	NP_054642.2:p.Arg51=
NM_013988.2:c.151A=	NP_054643.2:p.Arg51=
XM_011535863.1:c.151A=	XP_011534165.1:p.Arg51=
XM_011535864.1:c.151A=	XP_011534166.1:p.Arg51=
XM_011535865.1:c.151A=	XP_011534167.1:p.Arg51=
XM_011535866.1:c.151A=	XP_011534168.1:p.Arg51=
XM_011535867.1:c.151A=	XP_011534169.1:p.Arg51=
XM_017010908.1:c.265A=	XP_016866397.1:p.Arg89=
XM_017010909.2:c.-66-180565A=	XP_016866398.1:n.-66-180565A=
XM_024446449.1:c.-66-180565A=	XP_024302217.1:n.-66-180565A=
XR_001743443.2:n.257A=
NM_004562.3:c.151A= MANE Select	NP_004553.2:p.Arg51=
NM_013987.3:c.151A=	NP_054642.2:p.Arg51=
NM_013988.3:c.151A=	NP_054643.2:p.Arg51=