Canonical Allele Identifier: CA1677565100

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161512956A= , CM000668.2:g.161512956A=	GRCh38
NC_000006.11:g.161933988A= , CM000668.1:g.161933988A=	GRCh37
NC_000006.10:g.161853978A=	NCBI36
NG_008289.1:g.1219847T=
NG_008289.2:g.1219847T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.961+35898T=	ENSP00000343589.4:n.961+35898T=
ENST00000366894.6:c.842+35898T=	ENSP00000355860.2:n.842+35898T=
ENST00000366898.6:c.1083+35898T= MANE Select	ENSP00000355865.1:n.1083+35898T=
ENST00000673871.1:c.1078+35898T=
ENST00000674006.1:n.468+35898T=
ENST00000674436.1:n.719+35898T=
ENST00000674501.1:n.1190+35898T=
ENST00000338468.7:c.510+35898T=	ENSP00000343589.3:n.510+35898T=
ENST00000366894.5:c.510+35898T=	ENSP00000355860.1:n.510+35898T=
ENST00000366896.5:c.636+35898T=	ENSP00000355862.1:n.636+35898T=
ENST00000366897.5:c.999+35898T=	ENSP00000355863.1:n.999+35898T=
ENST00000366898.5:c.1083+35898T=	ENSP00000355865.1:n.1083+35898T=
ENST00000479615.5:c.635-126079T=	ENSP00000434414.1:n.635-126079T=
ENST00000610470.4:c.216+35898T=	ENSP00000483773.1:n.216+35898T=
NM_004562.2:c.1083+35898T=	NP_004553.2:n.1083+35898T=
NM_013987.2:c.999+35898T=	NP_054642.2:n.999+35898T=
NM_013988.2:c.636+35898T=	NP_054643.2:n.636+35898T=
XM_011535863.1:c.1080+35898T=	XP_011534165.1:n.1080+35898T=
XM_011535865.1:c.1083+35898T=	XP_011534167.1:n.1083+35898T=
XM_017010908.1:c.1197+35898T=	XP_016866397.1:n.1197+35898T=
XM_017010909.2:c.843+35898T=	XP_016866398.1:n.843+35898T=
XM_024446449.1:c.846+35898T=	XP_024302217.1:n.846+35898T=
XR_001743443.2:n.1189+35898T=
NM_004562.3:c.1083+35898T= MANE Select	NP_004553.2:n.1083+35898T=
NM_013987.3:c.999+35898T=	NP_054642.2:n.999+35898T=
NM_013988.3:c.636+35898T=	NP_054643.2:n.636+35898T=