Canonical Allele Identifier: CA1678012996

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443325_162443326delinsAT , CM000668.2:g.162443325_162443326delinsAT	GRCh38
NC_000006.11:g.162864357_162864358delinsAT , CM000668.1:g.162864357_162864358delinsAT	GRCh37
NC_000006.10:g.162784347_162784348delinsAT	NCBI36
NG_008289.1:g.289477_289478delinsAT
NG_008289.2:g.289477_289478delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.155_156delinsAT	ENSP00000343589.4:p.Asn52=
ENST00000366894.6:c.155_156delinsAT	ENSP00000355860.2:p.Asn52=
ENST00000366898.6:c.155_156delinsAT MANE Select	ENSP00000355865.1:p.Asn52=
ENST00000648830.1:n.322_323delinsAT
ENST00000673871.1:c.150_151delinsAT
ENST00000674232.1:n.173_174delinsAT
ENST00000674259.1:n.212_213delinsAT
ENST00000674493.1:n.172_173delinsAT
ENST00000674501.1:n.262_263delinsAT
ENST00000338468.7:c.-297_-296delinsAT	ENSP00000343589.3:n.-297_-296delinsAT
ENST00000366892.5:c.155_156delinsAT	ENSP00000355858.1:p.Asn52=
ENST00000366894.5:c.-178_-177delinsAT	ENSP00000355860.1:n.-178_-177delinsAT
ENST00000366896.5:c.155_156delinsAT	ENSP00000355862.1:p.Asn52=
ENST00000366897.5:c.155_156delinsAT	ENSP00000355863.1:p.Asn52=
ENST00000366898.5:c.155_156delinsAT	ENSP00000355865.1:p.Asn52=
ENST00000479615.5:c.-66-180561_-66-180560delinsAT	ENSP00000434414.1:n.-66-180561_-66-180560delinsAT
NM_004562.2:c.155_156delinsAT	NP_004553.2:p.Asn52=
NM_013987.2:c.155_156delinsAT	NP_054642.2:p.Asn52=
NM_013988.2:c.155_156delinsAT	NP_054643.2:p.Asn52=
XM_011535863.1:c.155_156delinsAT	XP_011534165.1:p.Asn52=
XM_011535864.1:c.155_156delinsAT	XP_011534166.1:p.Asn52=
XM_011535865.1:c.155_156delinsAT	XP_011534167.1:p.Asn52=
XM_011535866.1:c.155_156delinsAT	XP_011534168.1:p.Asn52=
XM_011535867.1:c.155_156delinsAT	XP_011534169.1:p.Asn52=
XM_017010908.1:c.269_270delinsAT	XP_016866397.1:p.Asn90=
XM_017010909.2:c.-66-180561_-66-180560delinsAT	XP_016866398.1:n.-66-180561_-66-180560delinsAT
XM_024446449.1:c.-66-180561_-66-180560delinsAT	XP_024302217.1:n.-66-180561_-66-180560delinsAT
XR_001743443.2:n.261_262delinsAT
NM_004562.3:c.155_156delinsAT MANE Select	NP_004553.2:p.Asn52=
NM_013987.3:c.155_156delinsAT	NP_054642.2:p.Asn52=
NM_013988.3:c.155_156delinsAT	NP_054643.2:p.Asn52=