Canonical Allele Identifier: CA1678013095

Gene: PRKN

Linked Data

• dbSNP Id: rs1790164143

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443514del , CM000668.2:g.162443514del	GRCh38
NC_000006.11:g.162864546del , CM000668.1:g.162864546del	GRCh37
NC_000006.10:g.162784536del	NCBI36
NG_008289.1:g.289289del
NG_008289.2:g.289289del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.8-41del	ENSP00000343589.4:n.8-41del
ENST00000366894.6:c.8-41del	ENSP00000355860.2:n.8-41del
ENST00000366898.6:c.8-41del MANE Select	ENSP00000355865.1:n.8-41del
ENST00000648830.1:n.175-41del
ENST00000674232.1:n.26-41del
ENST00000674259.1:n.65-41del
ENST00000674493.1:n.25-41del
ENST00000674501.1:n.115-41del
ENST00000338468.7:c.-444-41del	ENSP00000343589.3:n.-444-41del
ENST00000366892.5:c.8-41del	ENSP00000355858.1:n.8-41del
ENST00000366894.5:c.-325-41del	ENSP00000355860.1:n.-325-41del
ENST00000366896.5:c.8-41del	ENSP00000355862.1:n.8-41del
ENST00000366897.5:c.8-41del	ENSP00000355863.1:n.8-41del
ENST00000366898.5:c.8-41del	ENSP00000355865.1:n.8-41del
ENST00000479615.5:c.-66-180749del	ENSP00000434414.1:n.-66-180749del
NM_004562.2:c.8-41del	NP_004553.2:n.8-41del
NM_013987.2:c.8-41del	NP_054642.2:n.8-41del
NM_013988.2:c.8-41del	NP_054643.2:n.8-41del
XM_011535863.1:c.8-41del	XP_011534165.1:n.8-41del
XM_011535864.1:c.8-41del	XP_011534166.1:n.8-41del
XM_011535865.1:c.8-41del	XP_011534167.1:n.8-41del
XM_011535866.1:c.8-41del	XP_011534168.1:n.8-41del
XM_011535867.1:c.8-41del	XP_011534169.1:n.8-41del
XM_017010908.1:c.122-41del	XP_016866397.1:n.122-41del
XM_017010909.2:c.-66-180749del	XP_016866398.1:n.-66-180749del
XM_024446449.1:c.-66-180749del	XP_024302217.1:n.-66-180749del
XR_001743443.2:n.114-41del
NM_004562.3:c.8-41del MANE Select	NP_004553.2:n.8-41del
NM_013987.3:c.8-41del	NP_054642.2:n.8-41del
NM_013988.3:c.8-41del	NP_054643.2:n.8-41del