Canonical Allele Identifier: CA1365200608

Gene: PRKCD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53178427C= , CM000665.2:g.53178427C=	GRCh38
NC_000003.11:g.53212443C= , CM000665.1:g.53212443C=	GRCh37
NC_000003.10:g.53187483C=	NCBI36
NG_033864.1:g.22221C=
NG_033864.2:g.27419C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006254.4:c.5C= MANE Select	NP_006245.2:p.Ala2=
ENST00000330452.8:c.5C= MANE Select	ENSP00000331602.3:p.Ala2=
NM_001316327.1:c.5C=	NP_001303256.1:p.Ala2=
NM_001316327.2:c.5C=	NP_001303256.1:p.Ala2=
NM_001354676.1:c.62C=	NP_001341605.1:p.Ala21=
NM_001354676.2:c.62C=	NP_001341605.1:p.Ala21=
NM_001354678.1:c.53C=	NP_001341607.1:p.Ala18=
NM_001354678.2:c.53C=	NP_001341607.1:p.Ala18=
NM_001354679.1:c.5C=	NP_001341608.1:p.Ala2=
NM_001354679.2:c.5C=	NP_001341608.1:p.Ala2=
NM_001354680.1:c.5C=	NP_001341609.1:p.Ala2=
NM_001354680.2:c.5C=	NP_001341609.1:p.Ala2=
NM_006254.3:c.5C=	NP_006245.2:p.Ala2=
NM_212539.1:c.5C=	NP_997704.1:p.Ala2=
NM_212539.2:c.5C=	NP_997704.1:p.Ala2=
ENST00000330452.7:c.5C=	ENSP00000331602.3:p.Ala2=
ENST00000394729.6:c.5C=	ENSP00000378217.2:p.Ala2=
ENST00000464818.1:c.5C=	ENSP00000419629.1:p.Ala2=
ENST00000477794.2:n.294C=
ENST00000478843.5:c.5C=	ENSP00000419726.1:p.Ala2=
ENST00000487897.5:c.5C=	ENSP00000418106.1:p.Ala2=
ENST00000650739.1:c.5C=	ENSP00000498623.1:p.Ala2=
ENST00000650940.1:c.5C=	ENSP00000499184.1:p.Ala2=
ENST00000652449.1:c.5C=	ENSP00000498400.1:p.Ala2=
ENST00000654719.1:c.5C=	ENSP00000499558.1:p.Ala2=
ENST00000697588.1:c.5C=	ENSP00000513355.1:p.Ala2=
XM_006713257.2:c.53C=	XP_006713320.1:p.Ala18=
XM_006713259.2:c.5C=	XP_006713322.1:p.Ala2=
XR_002959550.1:n.77C=
XR_940474.1:n.24C=