Canonical Allele Identifier: CA453046196

Gene: PRKN

Linked Data

• MyVariant Identifiers: chr6:g.161771152C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161350120C>G , CM000668.2:g.161350120C>G	GRCh38
NC_000006.11:g.161771152C>G , CM000668.1:g.161771152C>G	GRCh37
NC_000006.10:g.161691142C>G	NCBI36
NG_008289.1:g.1382683G>C
NG_008289.2:g.1382683G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000338468.8:c.1255G>C	ENSP00000343589.4:n.1255G>C
ENST00000366894.6:c.1136G>C	ENSP00000355860.2:n.1136G>C
ENST00000366898.6:c.1377G>C MANE Select	ENSP00000355865.1:p.Gly459=
ENST00000673871.1:c.1458G>C
ENST00000674006.1:n.762G>C
ENST00000674436.1:n.1013G>C
ENST00000338468.7:c.804G>C	ENSP00000343589.3:p.Gly268=
ENST00000366894.5:c.804G>C	ENSP00000355860.1:p.Gly268=
ENST00000366896.5:c.930G>C	ENSP00000355862.1:p.Gly310=
ENST00000366897.5:c.1293G>C	ENSP00000355863.1:p.Gly431=
ENST00000366898.5:c.1377G>C	ENSP00000355865.1:p.Gly459=
ENST00000479615.5:c.*153G>C	ENSP00000434414.1:n.*153G>C
ENST00000610470.4:c.510G>C	ENSP00000483773.1:p.Gly170=
NM_004562.2:c.1377G>C	NP_004553.2:p.Gly459=
NM_013987.2:c.1293G>C	NP_054642.2:p.Gly431=
NM_013988.2:c.930G>C	NP_054643.2:p.Gly310=
XM_011535863.1:c.1374G>C	XP_011534165.1:p.Gly458=
XM_017010908.1:c.1491G>C	XP_016866397.1:p.Gly497=
XM_017010909.2:c.1137G>C	XP_016866398.1:p.Gly379=
XM_024446449.1:c.1140G>C	XP_024302217.1:p.Gly380=
XR_001743443.2:n.1569G>C
NM_004562.3:c.1377G>C MANE Select	NP_004553.2:p.Gly459=
NM_013987.3:c.1293G>C	NP_054642.2:p.Gly431=
NM_013988.3:c.930G>C	NP_054643.2:p.Gly310=