Canonical Allele Identifier: CA2126414937

Gene: PRKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626506T= , CM000676.2:g.29626506T=	GRCh38
NC_000014.8:g.30095712T= , CM000676.1:g.30095712T=	GRCh37
NC_000014.7:g.29165463T=	NCBI36
NG_052879.1:g.306188A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1547A=
ENST00000691517.1:n.1060A=
ENST00000331968.11:c.1776A= MANE Select	ENSP00000333568.6:p.Gly592=
ENST00000651571.1:c.1588A=	ENSP00000498919.1:n.1588A=
ENST00000651616.1:c.1657A=	ENSP00000498661.1:n.1657A=
ENST00000331968.9:c.1776A=	ENSP00000333568.5:p.Gly592=
ENST00000415220.6:c.1800A=	ENSP00000390535.2:p.Gly600=
ENST00000616995.4:c.1776A=	ENSP00000482645.1:p.Gly592=
NM_002742.2:c.1776A=	NP_002733.2:p.Gly592=
XM_005267859.1:c.1800A=	XP_005267916.1:p.Gly600=
XM_011536964.1:c.1572A=	XP_011535266.1:p.Gly524=
XM_011536965.1:c.1512A=	XP_011535267.1:p.Gly504=
XR_943493.1:n.1915A=
NM_001330069.1:c.1800A=	NP_001316998.1:p.Gly600=
NM_001348390.1:c.1512A=	NP_001335319.1:p.Gly504=
XM_011536965.2:c.1512A=	XP_011535267.1:p.Gly504=
XM_017021462.1:c.1281A=	XP_016876951.1:p.Gly427=
XR_943493.2:n.2093A=
NM_001330069.2:c.1800A=	NP_001316998.1:p.Gly600=
NM_002742.3:c.1776A= MANE Select	NP_002733.2:p.Gly592=