Canonical Allele Identifier: CA2578792196

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443530del , CM000668.2:g.162443530del	GRCh38
NC_000006.11:g.162864562del , CM000668.1:g.162864562del	GRCh37
NC_000006.10:g.162784552del	NCBI36
NG_008289.1:g.289275del
NG_008289.2:g.289275del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.8-55del	ENSP00000343589.4:n.8-55del
ENST00000366894.6:c.8-55del	ENSP00000355860.2:n.8-55del
ENST00000366898.6:c.8-55del MANE Select	ENSP00000355865.1:n.8-55del
ENST00000648830.1:n.175-55del
ENST00000674232.1:n.26-55del
ENST00000674259.1:n.65-55del
ENST00000674493.1:n.25-55del
ENST00000674501.1:n.115-55del
ENST00000338468.7:c.-444-55del	ENSP00000343589.3:n.-444-55del
ENST00000366892.5:c.8-55del	ENSP00000355858.1:n.8-55del
ENST00000366894.5:c.-325-55del	ENSP00000355860.1:n.-325-55del
ENST00000366896.5:c.8-55del	ENSP00000355862.1:n.8-55del
ENST00000366897.5:c.8-55del	ENSP00000355863.1:n.8-55del
ENST00000366898.5:c.8-55del	ENSP00000355865.1:n.8-55del
ENST00000479615.5:c.-66-180763del	ENSP00000434414.1:n.-66-180763del
NM_004562.2:c.8-55del	NP_004553.2:n.8-55del
NM_013987.2:c.8-55del	NP_054642.2:n.8-55del
NM_013988.2:c.8-55del	NP_054643.2:n.8-55del
XM_011535863.1:c.8-55del	XP_011534165.1:n.8-55del
XM_011535864.1:c.8-55del	XP_011534166.1:n.8-55del
XM_011535865.1:c.8-55del	XP_011534167.1:n.8-55del
XM_011535866.1:c.8-55del	XP_011534168.1:n.8-55del
XM_011535867.1:c.8-55del	XP_011534169.1:n.8-55del
XM_017010908.1:c.122-55del	XP_016866397.1:n.122-55del
XM_017010909.2:c.-66-180763del	XP_016866398.1:n.-66-180763del
XM_024446449.1:c.-66-180763del	XP_024302217.1:n.-66-180763del
XR_001743443.2:n.114-55del
NM_004562.3:c.8-55del MANE Select	NP_004553.2:n.8-55del
NM_013987.3:c.8-55del	NP_054642.2:n.8-55del
NM_013988.3:c.8-55del	NP_054643.2:n.8-55del