Canonical Allele Identifier: CA453046207

Gene: PRKN

Linked Data

• MyVariant Identifiers: chr6:g.161771179G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161350147G>C , CM000668.2:g.161350147G>C	GRCh38
NC_000006.11:g.161771179G>C , CM000668.1:g.161771179G>C	GRCh37
NC_000006.10:g.161691169G>C	NCBI36
NG_008289.1:g.1382656C>G
NG_008289.2:g.1382656C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000338468.8:c.1228C>G	ENSP00000343589.4:n.1228C>G
ENST00000366894.6:c.1109C>G	ENSP00000355860.2:n.1109C>G
ENST00000366898.6:c.1350C>G MANE Select	ENSP00000355865.1:p.Gly450=
ENST00000673871.1:c.1431C>G
ENST00000674006.1:n.735C>G
ENST00000674436.1:n.986C>G
ENST00000338468.7:c.777C>G	ENSP00000343589.3:p.Gly259=
ENST00000366894.5:c.777C>G	ENSP00000355860.1:p.Gly259=
ENST00000366896.5:c.903C>G	ENSP00000355862.1:p.Gly301=
ENST00000366897.5:c.1266C>G	ENSP00000355863.1:p.Gly422=
ENST00000366898.5:c.1350C>G	ENSP00000355865.1:p.Gly450=
ENST00000479615.5:c.*126C>G	ENSP00000434414.1:n.*126C>G
ENST00000610470.4:c.483C>G	ENSP00000483773.1:p.Gly161=
NM_004562.2:c.1350C>G	NP_004553.2:p.Gly450=
NM_013987.2:c.1266C>G	NP_054642.2:p.Gly422=
NM_013988.2:c.903C>G	NP_054643.2:p.Gly301=
XM_011535863.1:c.1347C>G	XP_011534165.1:p.Gly449=
XM_017010908.1:c.1464C>G	XP_016866397.1:p.Gly488=
XM_017010909.2:c.1110C>G	XP_016866398.1:p.Gly370=
XM_024446449.1:c.1113C>G	XP_024302217.1:p.Gly371=
XR_001743443.2:n.1542C>G
NM_004562.3:c.1350C>G MANE Select	NP_004553.2:p.Gly450=
NM_013987.3:c.1266C>G	NP_054642.2:p.Gly422=
NM_013988.3:c.903C>G	NP_054643.2:p.Gly301=