Canonical Allele Identifier: CA389334069

Gene: PRKD1

Linked Data

• MyVariant Identifiers: chr14:g.30095738A>G (hg19) ; chr14:g.29626532A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626532A>G , CM000676.2:g.29626532A>G	GRCh38
NC_000014.8:g.30095738A>G , CM000676.1:g.30095738A>G	GRCh37
NC_000014.7:g.29165489A>G	NCBI36
NG_052879.1:g.306162T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1521T>C
ENST00000691517.1:n.1034T>C
ENST00000331968.11:c.1750T>C MANE Select	ENSP00000333568.6:p.Phe584Leu
ENST00000651571.1:c.1562T>C	ENSP00000498919.1:n.1562T>C
ENST00000651616.1:c.1631T>C	ENSP00000498661.1:n.1631T>C
ENST00000331968.9:c.1750T>C	ENSP00000333568.5:p.Phe584Leu
ENST00000415220.6:c.1774T>C	ENSP00000390535.2:p.Phe592Leu
ENST00000616995.4:c.1750T>C	ENSP00000482645.1:p.Phe584Leu
NM_002742.2:c.1750T>C	NP_002733.2:p.Phe584Leu
XM_005267859.1:c.1774T>C	XP_005267916.1:p.Phe592Leu
XM_011536964.1:c.1546T>C	XP_011535266.1:p.Phe516Leu
XM_011536965.1:c.1486T>C	XP_011535267.1:p.Phe496Leu
XR_943493.1:n.1889T>C
NM_001330069.1:c.1774T>C	NP_001316998.1:p.Phe592Leu
NM_001348390.1:c.1486T>C	NP_001335319.1:p.Phe496Leu
XM_011536965.2:c.1486T>C	XP_011535267.1:p.Phe496Leu
XM_017021462.1:c.1255T>C	XP_016876951.1:p.Phe419Leu
XR_943493.2:n.2067T>C
NM_001330069.2:c.1774T>C	NP_001316998.1:p.Phe592Leu
NM_002742.3:c.1750T>C MANE Select	NP_002733.2:p.Phe584Leu