Canonical Allele Identifier: CA821730574

Gene: PRKN

Linked Data

• dbSNP Id: rs1352618741
• MyVariant Identifiers: chr6:g.161933928_161933929insAT (hg19) ; chr6:g.161512896_161512897insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161512899_161512900dup , CM000668.2:g.161512899_161512900dup	GRCh38
NC_000006.11:g.161933931_161933932dup , CM000668.1:g.161933931_161933932dup	GRCh37
NC_000006.10:g.161853921_161853922dup	NCBI36
NG_008289.1:g.1219905_1219906dup
NG_008289.2:g.1219905_1219906dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.961+35956_961+35957dup	ENSP00000343589.4:n.961+35956_961+35957dup
ENST00000366894.6:c.842+35956_842+35957dup	ENSP00000355860.2:n.842+35956_842+35957dup
ENST00000366898.6:c.1083+35956_1083+35957dup MANE Select	ENSP00000355865.1:n.1083+35956_1083+35957dup
ENST00000673871.1:c.1078+35956_1078+35957dup
ENST00000674006.1:n.468+35956_468+35957dup
ENST00000674436.1:n.719+35956_719+35957dup
ENST00000674501.1:n.1190+35956_1190+35957dup
ENST00000338468.7:c.510+35956_510+35957dup	ENSP00000343589.3:n.510+35956_510+35957dup
ENST00000366894.5:c.510+35956_510+35957dup	ENSP00000355860.1:n.510+35956_510+35957dup
ENST00000366896.5:c.636+35956_636+35957dup	ENSP00000355862.1:n.636+35956_636+35957dup
ENST00000366897.5:c.999+35956_999+35957dup	ENSP00000355863.1:n.999+35956_999+35957dup
ENST00000366898.5:c.1083+35956_1083+35957dup	ENSP00000355865.1:n.1083+35956_1083+35957dup
ENST00000479615.5:c.635-126021_635-126020dup	ENSP00000434414.1:n.635-126021_635-126020dup
ENST00000610470.4:c.216+35956_216+35957dup	ENSP00000483773.1:n.216+35956_216+35957dup
NM_004562.2:c.1083+35956_1083+35957dup	NP_004553.2:n.1083+35956_1083+35957dup
NM_013987.2:c.999+35956_999+35957dup	NP_054642.2:n.999+35956_999+35957dup
NM_013988.2:c.636+35956_636+35957dup	NP_054643.2:n.636+35956_636+35957dup
XM_011535863.1:c.1080+35956_1080+35957dup	XP_011534165.1:n.1080+35956_1080+35957dup
XM_011535865.1:c.1083+35956_1083+35957dup	XP_011534167.1:n.1083+35956_1083+35957dup
XM_017010908.1:c.1197+35956_1197+35957dup	XP_016866397.1:n.1197+35956_1197+35957dup
XM_017010909.2:c.843+35956_843+35957dup	XP_016866398.1:n.843+35956_843+35957dup
XM_024446449.1:c.846+35956_846+35957dup	XP_024302217.1:n.846+35956_846+35957dup
XR_001743443.2:n.1189+35956_1189+35957dup
NM_004562.3:c.1083+35956_1083+35957dup MANE Select	NP_004553.2:n.1083+35956_1083+35957dup
NM_013987.3:c.999+35956_999+35957dup	NP_054642.2:n.999+35956_999+35957dup
NM_013988.3:c.636+35956_636+35957dup	NP_054643.2:n.636+35956_636+35957dup