Canonical Allele Identifier: CA389334065

Gene: PRKD1

Linked Data

• MyVariant Identifiers: chr14:g.30095737A>T (hg19) ; chr14:g.29626531A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626531A>T , CM000676.2:g.29626531A>T	GRCh38
NC_000014.8:g.30095737A>T , CM000676.1:g.30095737A>T	GRCh37
NC_000014.7:g.29165488A>T	NCBI36
NG_052879.1:g.306163T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1522T>A
ENST00000691517.1:n.1035T>A
ENST00000331968.11:c.1751T>A MANE Select	ENSP00000333568.6:p.Phe584Tyr
ENST00000651571.1:c.1563T>A	ENSP00000498919.1:n.1563T>A
ENST00000651616.1:c.1632T>A	ENSP00000498661.1:n.1632T>A
ENST00000331968.9:c.1751T>A	ENSP00000333568.5:p.Phe584Tyr
ENST00000415220.6:c.1775T>A	ENSP00000390535.2:p.Phe592Tyr
ENST00000616995.4:c.1751T>A	ENSP00000482645.1:p.Phe584Tyr
NM_002742.2:c.1751T>A	NP_002733.2:p.Phe584Tyr
XM_005267859.1:c.1775T>A	XP_005267916.1:p.Phe592Tyr
XM_011536964.1:c.1547T>A	XP_011535266.1:p.Phe516Tyr
XM_011536965.1:c.1487T>A	XP_011535267.1:p.Phe496Tyr
XR_943493.1:n.1890T>A
NM_001330069.1:c.1775T>A	NP_001316998.1:p.Phe592Tyr
NM_001348390.1:c.1487T>A	NP_001335319.1:p.Phe496Tyr
XM_011536965.2:c.1487T>A	XP_011535267.1:p.Phe496Tyr
XM_017021462.1:c.1256T>A	XP_016876951.1:p.Phe419Tyr
XR_943493.2:n.2068T>A
NM_001330069.2:c.1775T>A	NP_001316998.1:p.Phe592Tyr
NM_002742.3:c.1751T>A MANE Select	NP_002733.2:p.Phe584Tyr