Canonical Allele Identifier: CA485824943

Gene: PRKD1

Linked Data

• MyVariant Identifiers: chr14:g.30095709C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626503C>T , CM000676.2:g.29626503C>T	GRCh38
NC_000014.8:g.30095709C>T , CM000676.1:g.30095709C>T	GRCh37
NC_000014.7:g.29165460C>T	NCBI36
NG_052879.1:g.306191G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1550G>A
ENST00000691517.1:n.1063G>A
ENST00000331968.11:c.1779G>A MANE Select	ENSP00000333568.6:p.Gln593=
ENST00000651571.1:c.1591G>A	ENSP00000498919.1:n.1591G>A
ENST00000651616.1:c.1660G>A	ENSP00000498661.1:n.1660G>A
ENST00000331968.9:c.1779G>A	ENSP00000333568.5:p.Gln593=
ENST00000415220.6:c.1803G>A	ENSP00000390535.2:p.Gln601=
ENST00000616995.4:c.1779G>A	ENSP00000482645.1:p.Gln593=
NM_002742.2:c.1779G>A	NP_002733.2:p.Gln593=
XM_005267859.1:c.1803G>A	XP_005267916.1:p.Gln601=
XM_011536964.1:c.1575G>A	XP_011535266.1:p.Gln525=
XM_011536965.1:c.1515G>A	XP_011535267.1:p.Gln505=
XR_943493.1:n.1918G>A
NM_001330069.1:c.1803G>A	NP_001316998.1:p.Gln601=
NM_001348390.1:c.1515G>A	NP_001335319.1:p.Gln505=
XM_011536965.2:c.1515G>A	XP_011535267.1:p.Gln505=
XM_017021462.1:c.1284G>A	XP_016876951.1:p.Gln428=
XR_943493.2:n.2096G>A
NM_001330069.2:c.1803G>A	NP_001316998.1:p.Gln601=
NM_002742.3:c.1779G>A MANE Select	NP_002733.2:p.Gln593=