Canonical Allele Identifier: CA2126414936

Gene: PRKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626502A= , CM000676.2:g.29626502A=	GRCh38
NC_000014.8:g.30095708A= , CM000676.1:g.30095708A=	GRCh37
NC_000014.7:g.29165459A=	NCBI36
NG_052879.1:g.306192T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1551T=
ENST00000691517.1:n.1064T=
ENST00000331968.11:c.1780T= MANE Select	ENSP00000333568.6:p.Phe594=
ENST00000651571.1:c.1592T=	ENSP00000498919.1:n.1592T=
ENST00000651616.1:c.1661T=	ENSP00000498661.1:n.1661T=
ENST00000331968.9:c.1780T=	ENSP00000333568.5:p.Phe594=
ENST00000415220.6:c.1804T=	ENSP00000390535.2:p.Phe602=
ENST00000616995.4:c.1780T=	ENSP00000482645.1:p.Phe594=
NM_002742.2:c.1780T=	NP_002733.2:p.Phe594=
XM_005267859.1:c.1804T=	XP_005267916.1:p.Phe602=
XM_011536964.1:c.1576T=	XP_011535266.1:p.Phe526=
XM_011536965.1:c.1516T=	XP_011535267.1:p.Phe506=
XR_943493.1:n.1919T=
NM_001330069.1:c.1804T=	NP_001316998.1:p.Phe602=
NM_001348390.1:c.1516T=	NP_001335319.1:p.Phe506=
XM_011536965.2:c.1516T=	XP_011535267.1:p.Phe506=
XM_017021462.1:c.1285T=	XP_016876951.1:p.Phe429=
XR_943493.2:n.2097T=
NM_001330069.2:c.1804T=	NP_001316998.1:p.Phe602=
NM_002742.3:c.1780T= MANE Select	NP_002733.2:p.Phe594=