Canonical Allele Identifier: CA1678012999

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443327_162443340delinsTCCTCAGCTCCTTC , CM000668.2:g.162443327_162443340delinsTCCTCAGCTCCTTC	GRCh38
NC_000006.11:g.162864359_162864372delinsTCCTCAGCTCCTTC , CM000668.1:g.162864359_162864372delinsTCCTCAGCTCCTTC	GRCh37
NC_000006.10:g.162784349_162784362delinsTCCTCAGCTCCTTC	NCBI36
NG_008289.1:g.289463_289476delinsGAAGGAGCTGAGGA
NG_008289.2:g.289463_289476delinsGAAGGAGCTGAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.141_154delinsGAAGGAGCTGAGGA	ENSP00000343589.4:p.Gly47=
ENST00000366894.6:c.141_154delinsGAAGGAGCTGAGGA	ENSP00000355860.2:p.Gly47=
ENST00000366898.6:c.141_154delinsGAAGGAGCTGAGGA MANE Select	ENSP00000355865.1:p.Gly47=
ENST00000648830.1:n.308_321delinsGAAGGAGCTGAGGA
ENST00000673871.1:c.136_149delinsGAAGGAGCTGAGGA
ENST00000674232.1:n.159_172delinsGAAGGAGCTGAGGA
ENST00000674259.1:n.198_211delinsGAAGGAGCTGAGGA
ENST00000674493.1:n.158_171delinsGAAGGAGCTGAGGA
ENST00000674501.1:n.248_261delinsGAAGGAGCTGAGGA
ENST00000338468.7:c.-311_-298delinsGAAGGAGCTGAGGA	ENSP00000343589.3:n.-311_-298delinsGAAGGAGCTGAGGA
ENST00000366892.5:c.141_154delinsGAAGGAGCTGAGGA	ENSP00000355858.1:p.Gly47=
ENST00000366894.5:c.-192_-179delinsGAAGGAGCTGAGGA	ENSP00000355860.1:n.-192_-179delinsGAAGGAGCTGAGGA
ENST00000366896.5:c.141_154delinsGAAGGAGCTGAGGA	ENSP00000355862.1:p.Gly47=
ENST00000366897.5:c.141_154delinsGAAGGAGCTGAGGA	ENSP00000355863.1:p.Gly47=
ENST00000366898.5:c.141_154delinsGAAGGAGCTGAGGA	ENSP00000355865.1:p.Gly47=
ENST00000479615.5:c.-66-180575_-66-180562delinsGAAGGAGCTGAGGA	ENSP00000434414.1:n.-66-180575_-66-180562delinsGAAGGAGCTGAGGA...
NM_004562.2:c.141_154delinsGAAGGAGCTGAGGA	NP_004553.2:p.Gly47=
NM_013987.2:c.141_154delinsGAAGGAGCTGAGGA	NP_054642.2:p.Gly47=
NM_013988.2:c.141_154delinsGAAGGAGCTGAGGA	NP_054643.2:p.Gly47=
XM_011535863.1:c.141_154delinsGAAGGAGCTGAGGA	XP_011534165.1:p.Gly47=
XM_011535864.1:c.141_154delinsGAAGGAGCTGAGGA	XP_011534166.1:p.Gly47=
XM_011535865.1:c.141_154delinsGAAGGAGCTGAGGA	XP_011534167.1:p.Gly47=
XM_011535866.1:c.141_154delinsGAAGGAGCTGAGGA	XP_011534168.1:p.Gly47=
XM_011535867.1:c.141_154delinsGAAGGAGCTGAGGA	XP_011534169.1:p.Gly47=
XM_017010908.1:c.255_268delinsGAAGGAGCTGAGGA	XP_016866397.1:p.Gly85=
XM_017010909.2:c.-66-180575_-66-180562delinsGAAGGAGCTGAGGA	XP_016866398.1:n.-66-180575_-66-180562delinsGAAGGAGCTGAGGA
XM_024446449.1:c.-66-180575_-66-180562delinsGAAGGAGCTGAGGA	XP_024302217.1:n.-66-180575_-66-180562delinsGAAGGAGCTGAGGA
XR_001743443.2:n.247_260delinsGAAGGAGCTGAGGA
NM_004562.3:c.141_154delinsGAAGGAGCTGAGGA MANE Select	NP_004553.2:p.Gly47=
NM_013987.3:c.141_154delinsGAAGGAGCTGAGGA	NP_054642.2:p.Gly47=
NM_013988.3:c.141_154delinsGAAGGAGCTGAGGA	NP_054643.2:p.Gly47=