Canonical Allele Identifier: CA2126414938

Gene: PRKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626508C= , CM000676.2:g.29626508C=	GRCh38
NC_000014.8:g.30095714C= , CM000676.1:g.30095714C=	GRCh37
NC_000014.7:g.29165465C=	NCBI36
NG_052879.1:g.306186G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1545G=
ENST00000691517.1:n.1058G=
ENST00000331968.11:c.1774G= MANE Select	ENSP00000333568.6:p.Gly592=
ENST00000651571.1:c.1586G=	ENSP00000498919.1:n.1586G=
ENST00000651616.1:c.1655G=	ENSP00000498661.1:n.1655G=
ENST00000331968.9:c.1774G=	ENSP00000333568.5:p.Gly592=
ENST00000415220.6:c.1798G=	ENSP00000390535.2:p.Gly600=
ENST00000616995.4:c.1774G=	ENSP00000482645.1:p.Gly592=
NM_002742.2:c.1774G=	NP_002733.2:p.Gly592=
XM_005267859.1:c.1798G=	XP_005267916.1:p.Gly600=
XM_011536964.1:c.1570G=	XP_011535266.1:p.Gly524=
XM_011536965.1:c.1510G=	XP_011535267.1:p.Gly504=
XR_943493.1:n.1913G=
NM_001330069.1:c.1798G=	NP_001316998.1:p.Gly600=
NM_001348390.1:c.1510G=	NP_001335319.1:p.Gly504=
XM_011536965.2:c.1510G=	XP_011535267.1:p.Gly504=
XM_017021462.1:c.1279G=	XP_016876951.1:p.Gly427=
XR_943493.2:n.2091G=
NM_001330069.2:c.1798G=	NP_001316998.1:p.Gly600=
NM_002742.3:c.1774G= MANE Select	NP_002733.2:p.Gly592=