Canonical Allele Identifier: CA1677891119

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162201134G= , CM000668.2:g.162201134G=	GRCh38
NC_000006.11:g.162622166G= , CM000668.1:g.162622166G=	GRCh37
NC_000006.10:g.162542156G=	NCBI36
NG_008289.1:g.531669C=
NG_008289.2:g.531669C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000338468.8:c.412+61391C=	ENSP00000343589.4:n.412+61391C=
ENST00000366894.6:c.290C=	ENSP00000355860.2:n.290C=
ENST00000366898.6:c.531C= MANE Select	ENSP00000355865.1:p.Thr177=
ENST00000673871.1:c.526C=
ENST00000674232.1:n.549C=
ENST00000674436.1:n.167C=
ENST00000674501.1:n.638C=
ENST00000338468.7:c.-40+61391C=	ENSP00000343589.3:n.-40+61391C=
ENST00000366892.5:c.531C=	ENSP00000355858.1:p.Thr177=
ENST00000366894.5:c.-43C=	ENSP00000355860.1:n.-43C=
ENST00000366896.5:c.172-227717C=	ENSP00000355862.1:n.172-227717C=
ENST00000366897.5:c.531C=	ENSP00000355863.1:p.Thr177=
ENST00000366898.5:c.531C=	ENSP00000355865.1:p.Thr177=
ENST00000479615.5:c.294C=	ENSP00000434414.1:p.Thr98=
NM_004562.2:c.531C=	NP_004553.2:p.Thr177=
NM_013987.2:c.531C=	NP_054642.2:p.Thr177=
NM_013988.2:c.172-227717C=	NP_054643.2:n.172-227717C=
XM_011535863.1:c.528C=	XP_011534165.1:p.Thr176=
XM_011535864.1:c.531C=	XP_011534166.1:p.Thr177=
XM_011535865.1:c.531C=	XP_011534167.1:p.Thr177=
XM_011535866.1:c.531C=	XP_011534168.1:p.Thr177=
XM_011535867.1:c.531C=	XP_011534169.1:p.Thr177=
XM_017010908.1:c.645C=	XP_016866397.1:p.Thr215=
XM_017010909.2:c.291C=	XP_016866398.1:p.Thr97=
XM_024446449.1:c.294C=	XP_024302217.1:p.Thr98=
XR_001743443.2:n.637C=
NM_004562.3:c.531C= MANE Select	NP_004553.2:p.Thr177=
NM_013987.3:c.531C=	NP_054642.2:p.Thr177=
NM_013988.3:c.172-227717C=	NP_054643.2:n.172-227717C=