Canonical Allele Identifier: CA1677459151

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161350019T= , CM000668.2:g.161350019T=	GRCh38
NC_000006.11:g.161771051T= , CM000668.1:g.161771051T=	GRCh37
NC_000006.10:g.161691041T=	NCBI36
NG_008289.1:g.1382784A=
NG_008289.2:g.1382784A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366898.6:c.*80A= MANE Select	ENSP00000355865.1:n.*80A=
ENST00000673871.1:c.1559A=
ENST00000674006.1:n.863A=
ENST00000674436.1:n.1114A=
ENST00000366896.5:c.*80A=	ENSP00000355862.1:n.*80A=
ENST00000366897.5:c.*80A=	ENSP00000355863.1:n.*80A=
ENST00000366898.5:c.*80A=	ENSP00000355865.1:n.*80A=
NM_004562.2:c.*80A=	NP_004553.2:n.*80A=
NM_013987.2:c.*80A=	NP_054642.2:n.*80A=
NM_013988.2:c.*80A=	NP_054643.2:n.*80A=
XM_011535863.1:c.*80A=	XP_011534165.1:n.*80A=
XM_017010908.1:c.*80A=	XP_016866397.1:n.*80A=
XM_017010909.2:c.*80A=	XP_016866398.1:n.*80A=
XM_024446449.1:c.*80A=	XP_024302217.1:n.*80A=
XR_001743443.2:n.1670A=
NM_004562.3:c.*80A= MANE Select	NP_004553.2:n.*80A=
NM_013987.3:c.*80A=	NP_054642.2:n.*80A=
NM_013988.3:c.*80A=	NP_054643.2:n.*80A=