Canonical Allele Identifier: CA2126414946

Gene: PRKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626533A= , CM000676.2:g.29626533A=	GRCh38
NC_000014.8:g.30095739A= , CM000676.1:g.30095739A=	GRCh37
NC_000014.7:g.29165490A=	NCBI36
NG_052879.1:g.306161T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1520T=
ENST00000691517.1:n.1033T=
ENST00000331968.11:c.1749T= MANE Select	ENSP00000333568.6:p.Ile583=
ENST00000651571.1:c.1561T=	ENSP00000498919.1:n.1561T=
ENST00000651616.1:c.1630T=	ENSP00000498661.1:n.1630T=
ENST00000331968.9:c.1749T=	ENSP00000333568.5:p.Ile583=
ENST00000415220.6:c.1773T=	ENSP00000390535.2:p.Ile591=
ENST00000616995.4:c.1749T=	ENSP00000482645.1:p.Ile583=
NM_002742.2:c.1749T=	NP_002733.2:p.Ile583=
XM_005267859.1:c.1773T=	XP_005267916.1:p.Ile591=
XM_011536964.1:c.1545T=	XP_011535266.1:p.Ile515=
XM_011536965.1:c.1485T=	XP_011535267.1:p.Ile495=
XR_943493.1:n.1888T=
NM_001330069.1:c.1773T=	NP_001316998.1:p.Ile591=
NM_001348390.1:c.1485T=	NP_001335319.1:p.Ile495=
XM_011536965.2:c.1485T=	XP_011535267.1:p.Ile495=
XM_017021462.1:c.1254T=	XP_016876951.1:p.Ile418=
XR_943493.2:n.2066T=
NM_001330069.2:c.1773T=	NP_001316998.1:p.Ile591=
NM_002742.3:c.1749T= MANE Select	NP_002733.2:p.Ile583=