Canonical Allele Identifier: CA2739279918

Gene: PRKCD

Linked Data

• ClinVar Variation Id: 2818526
• ClinVar RCV Id: RCV003744162

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53181684T>C , CM000665.2:g.53181684T>C	GRCh38
NC_000003.11:g.53215700T>C , CM000665.1:g.53215700T>C	GRCh37
NC_000003.10:g.53190740T>C	NCBI36
NG_033864.1:g.25478T>C
NG_033864.2:g.30676T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697588.1:c.540-17T>C	ENSP00000513355.1:n.540-17T>C
ENST00000330452.8:c.540-17T>C MANE Select	ENSP00000331602.3:n.540-17T>C
ENST00000650739.1:c.540-17T>C	ENSP00000498623.1:n.540-17T>C
ENST00000650940.1:c.540-17T>C	ENSP00000499184.1:n.540-17T>C
ENST00000651505.1:c.172-17T>C
ENST00000652449.1:c.540-17T>C	ENSP00000498400.1:n.540-17T>C
ENST00000654719.1:c.540-17T>C	ENSP00000499558.1:n.540-17T>C
ENST00000330452.7:c.540-17T>C	ENSP00000331602.3:n.540-17T>C
ENST00000394729.6:c.540-17T>C	ENSP00000378217.2:n.540-17T>C
ENST00000464818.1:c.540-17T>C	ENSP00000419629.1:n.540-17T>C
NM_001316327.1:c.540-17T>C	NP_001303256.1:n.540-17T>C
NM_006254.3:c.540-17T>C	NP_006245.2:n.540-17T>C
NM_212539.1:c.540-17T>C	NP_997704.1:n.540-17T>C
XM_006713257.2:c.588-17T>C	XP_006713320.1:n.588-17T>C
XM_006713259.2:c.540-17T>C	XP_006713322.1:n.540-17T>C
XR_940474.1:n.559-17T>C
NM_001354676.1:c.597-17T>C	NP_001341605.1:n.597-17T>C
NM_001354678.1:c.588-17T>C	NP_001341607.1:n.588-17T>C
NM_001354679.1:c.540-17T>C	NP_001341608.1:n.540-17T>C
NM_001354680.1:c.540-17T>C	NP_001341609.1:n.540-17T>C
XR_002959550.1:n.612-17T>C
NM_006254.4:c.540-17T>C MANE Select	NP_006245.2:n.540-17T>C
NM_001316327.2:c.540-17T>C	NP_001303256.1:n.540-17T>C
NM_001354676.2:c.597-17T>C	NP_001341605.1:n.597-17T>C
NM_001354678.2:c.588-17T>C	NP_001341607.1:n.588-17T>C
NM_001354679.2:c.540-17T>C	NP_001341608.1:n.540-17T>C
NM_001354680.2:c.540-17T>C	NP_001341609.1:n.540-17T>C
NM_212539.2:c.540-17T>C	NP_997704.1:n.540-17T>C