Canonical Allele Identifier: CA2681112479

Gene: PRKN

Linked Data

• gnomAD v4: 6-161349983-AGTGTGTGTGCGCGCGCGCGCGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161349993_161350014del , CM000668.2:g.161349993_161350014del	GRCh38
NC_000006.11:g.161771025_161771046del , CM000668.1:g.161771025_161771046del	GRCh37
NC_000006.10:g.161691015_161691036del	NCBI36
NG_008289.1:g.1382798_1382819del
NG_008289.2:g.1382798_1382819del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366898.6:c.*94_*115del MANE Select	ENSP00000355865.1:n.*94_*115del
ENST00000673871.1:c.1573_1594del
ENST00000674006.1:n.877_898del
ENST00000674436.1:n.1128_1149del
ENST00000366896.5:c.*94_*115del	ENSP00000355862.1:n.*94_*115del
ENST00000366897.5:c.*94_*115del	ENSP00000355863.1:n.*94_*115del
ENST00000366898.5:c.*94_*115del	ENSP00000355865.1:n.*94_*115del
NM_004562.2:c.*94_*115del	NP_004553.2:n.*94_*115del
NM_013987.2:c.*94_*115del	NP_054642.2:n.*94_*115del
NM_013988.2:c.*94_*115del	NP_054643.2:n.*94_*115del
XM_011535863.1:c.*94_*115del	XP_011534165.1:n.*94_*115del
XM_017010908.1:c.*94_*115del	XP_016866397.1:n.*94_*115del
XM_017010909.2:c.*94_*115del	XP_016866398.1:n.*94_*115del
XM_024446449.1:c.*94_*115del	XP_024302217.1:n.*94_*115del
XR_001743443.2:n.1684_1705del
NM_004562.3:c.*94_*115del MANE Select	NP_004553.2:n.*94_*115del
NM_013987.3:c.*94_*115del	NP_054642.2:n.*94_*115del
NM_013988.3:c.*94_*115del	NP_054643.2:n.*94_*115del