Canonical Allele Identifier: CA366475418

Gene: PRKN

Linked Data

• MyVariant Identifiers: chr6:g.162622167G>C (hg19) ; chr6:g.162201135G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.162201135G>C , CM000668.2:g.162201135G>C	GRCh38
NC_000006.11:g.162622167G>C , CM000668.1:g.162622167G>C	GRCh37
NC_000006.10:g.162542157G>C	NCBI36
NG_008289.1:g.531668C>G
NG_008289.2:g.531668C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000338468.8:c.412+61390C>G	ENSP00000343589.4:n.412+61390C>G
ENST00000366894.6:c.289C>G	ENSP00000355860.2:n.289C>G
ENST00000366898.6:c.530C>G MANE Select	ENSP00000355865.1:p.Thr177Ser
ENST00000673871.1:c.525C>G
ENST00000674232.1:n.548C>G
ENST00000674436.1:n.166C>G
ENST00000674501.1:n.637C>G
ENST00000338468.7:c.-40+61390C>G	ENSP00000343589.3:n.-40+61390C>G
ENST00000366892.5:c.530C>G	ENSP00000355858.1:p.Thr177Ser
ENST00000366894.5:c.-44C>G	ENSP00000355860.1:n.-44C>G
ENST00000366896.5:c.172-227718C>G	ENSP00000355862.1:n.172-227718C>G
ENST00000366897.5:c.530C>G	ENSP00000355863.1:p.Thr177Ser
ENST00000366898.5:c.530C>G	ENSP00000355865.1:p.Thr177Ser
ENST00000479615.5:c.293C>G	ENSP00000434414.1:p.Thr98Ser
NM_004562.2:c.530C>G	NP_004553.2:p.Thr177Ser
NM_013987.2:c.530C>G	NP_054642.2:p.Thr177Ser
NM_013988.2:c.172-227718C>G	NP_054643.2:n.172-227718C>G
XM_011535863.1:c.527C>G	XP_011534165.1:p.Thr176Ser
XM_011535864.1:c.530C>G	XP_011534166.1:p.Thr177Ser
XM_011535865.1:c.530C>G	XP_011534167.1:p.Thr177Ser
XM_011535866.1:c.530C>G	XP_011534168.1:p.Thr177Ser
XM_011535867.1:c.530C>G	XP_011534169.1:p.Thr177Ser
XM_017010908.1:c.644C>G	XP_016866397.1:p.Thr215Ser
XM_017010909.2:c.290C>G	XP_016866398.1:p.Thr97Ser
XM_024446449.1:c.293C>G	XP_024302217.1:p.Thr98Ser
XR_001743443.2:n.636C>G
NM_004562.3:c.530C>G MANE Select	NP_004553.2:p.Thr177Ser
NM_013987.3:c.530C>G	NP_054642.2:p.Thr177Ser
NM_013988.3:c.172-227718C>G	NP_054643.2:n.172-227718C>G