Canonical Allele Identifier: CA389333958

Gene: PRKD1

Linked Data

• COSMIC: COSM6275978 ; COSM6275979
• MyVariant Identifiers: chr14:g.30095711G>T (hg19) ; chr14:g.29626505G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626505G>T , CM000676.2:g.29626505G>T	GRCh38
NC_000014.8:g.30095711G>T , CM000676.1:g.30095711G>T	GRCh37
NC_000014.7:g.29165462G>T	NCBI36
NG_052879.1:g.306189C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1548C>A
ENST00000691517.1:n.1061C>A
ENST00000331968.11:c.1777C>A MANE Select	ENSP00000333568.6:p.Gln593Lys
ENST00000651571.1:c.1589C>A	ENSP00000498919.1:n.1589C>A
ENST00000651616.1:c.1658C>A	ENSP00000498661.1:n.1658C>A
ENST00000331968.9:c.1777C>A	ENSP00000333568.5:p.Gln593Lys
ENST00000415220.6:c.1801C>A	ENSP00000390535.2:p.Gln601Lys
ENST00000616995.4:c.1777C>A	ENSP00000482645.1:p.Gln593Lys
NM_002742.2:c.1777C>A	NP_002733.2:p.Gln593Lys
XM_005267859.1:c.1801C>A	XP_005267916.1:p.Gln601Lys
XM_011536964.1:c.1573C>A	XP_011535266.1:p.Gln525Lys
XM_011536965.1:c.1513C>A	XP_011535267.1:p.Gln505Lys
XR_943493.1:n.1916C>A
NM_001330069.1:c.1801C>A	NP_001316998.1:p.Gln601Lys
NM_001348390.1:c.1513C>A	NP_001335319.1:p.Gln505Lys
XM_011536965.2:c.1513C>A	XP_011535267.1:p.Gln505Lys
XM_017021462.1:c.1282C>A	XP_016876951.1:p.Gln428Lys
XR_943493.2:n.2094C>A
NM_001330069.2:c.1801C>A	NP_001316998.1:p.Gln601Lys
NM_002742.3:c.1777C>A MANE Select	NP_002733.2:p.Gln593Lys