Canonical Allele Identifier: CA366477438

Gene: PRKN

Linked Data

• ClinVar Variation Id: 2435249
• ClinVar RCV Id: RCV003135142
• dbSNP Id: rs1790160024
• MyVariant Identifiers: chr6:g.162864469A>G (hg19) ; chr6:g.162443437A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162443437A>G , CM000668.2:g.162443437A>G	GRCh38
NC_000006.11:g.162864469A>G , CM000668.1:g.162864469A>G	GRCh37
NC_000006.10:g.162784459A>G	NCBI36
NG_008289.1:g.289366T>C
NG_008289.2:g.289366T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.44T>C	ENSP00000343589.4:p.Val15Ala
ENST00000366894.6:c.44T>C	ENSP00000355860.2:p.Val15Ala
ENST00000366898.6:c.44T>C MANE Select	ENSP00000355865.1:p.Val15Ala
ENST00000648830.1:n.211T>C
ENST00000673871.1:c.39T>C
ENST00000674232.1:n.62T>C
ENST00000674259.1:n.101T>C
ENST00000674493.1:n.61T>C
ENST00000674501.1:n.151T>C
ENST00000338468.7:c.-408T>C	ENSP00000343589.3:n.-408T>C
ENST00000366892.5:c.44T>C	ENSP00000355858.1:p.Val15Ala
ENST00000366894.5:c.-289T>C	ENSP00000355860.1:n.-289T>C
ENST00000366896.5:c.44T>C	ENSP00000355862.1:p.Val15Ala
ENST00000366897.5:c.44T>C	ENSP00000355863.1:p.Val15Ala
ENST00000366898.5:c.44T>C	ENSP00000355865.1:p.Val15Ala
ENST00000479615.5:c.-66-180672T>C	ENSP00000434414.1:n.-66-180672T>C
NM_004562.2:c.44T>C	NP_004553.2:p.Val15Ala
NM_013987.2:c.44T>C	NP_054642.2:p.Val15Ala
NM_013988.2:c.44T>C	NP_054643.2:p.Val15Ala
XM_011535863.1:c.44T>C	XP_011534165.1:p.Val15Ala
XM_011535864.1:c.44T>C	XP_011534166.1:p.Val15Ala
XM_011535865.1:c.44T>C	XP_011534167.1:p.Val15Ala
XM_011535866.1:c.44T>C	XP_011534168.1:p.Val15Ala
XM_011535867.1:c.44T>C	XP_011534169.1:p.Val15Ala
XM_017010908.1:c.158T>C	XP_016866397.1:p.Val53Ala
XM_017010909.2:c.-66-180672T>C	XP_016866398.1:n.-66-180672T>C
XM_024446449.1:c.-66-180672T>C	XP_024302217.1:n.-66-180672T>C
XR_001743443.2:n.150T>C
NM_004562.3:c.44T>C MANE Select	NP_004553.2:p.Val15Ala
NM_013987.3:c.44T>C	NP_054642.2:p.Val15Ala
NM_013988.3:c.44T>C	NP_054643.2:p.Val15Ala