Canonical Allele Identifier: CA145457

Gene: PRKCD

Linked Data

• ClinVar Variation Id: 89076
• ClinVar RCV Id: RCV000074607
• dbSNP Id: rs398122958
• COSMIC: COSM3357735 ; COSM3357736
• MyVariant Identifiers: chr3:g.53220712G>A (hg19) ; chr3:g.53186696G>A (hg38)
• PubMed: PMID:23319571

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53186696G>A , CM000665.2:g.53186696G>A	GRCh38
NC_000003.11:g.53220712G>A , CM000665.1:g.53220712G>A	GRCh37
NC_000003.10:g.53195752G>A	NCBI36
NG_033864.1:g.30490G>A
NG_033864.2:g.35688G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697588.1:c.1353G>A	ENSP00000513355.1:p.Thr451=
ENST00000697589.1:n.1356+1G>A
ENST00000330452.8:c.1352+1G>A MANE Select	ENSP00000331602.3:n.1352+1G>A
ENST00000650739.1:c.1352+1G>A	ENSP00000498623.1:n.1352+1G>A
ENST00000651505.1:c.1093+1G>A
ENST00000652449.1:c.1352+1G>A	ENSP00000498400.1:n.1352+1G>A
ENST00000654719.1:c.1352+1G>A	ENSP00000499558.1:n.1352+1G>A
ENST00000330452.7:c.1352+1G>A	ENSP00000331602.3:n.1352+1G>A
ENST00000394729.6:c.1352+1G>A	ENSP00000378217.2:n.1352+1G>A
NM_001316327.1:c.1352+1G>A	NP_001303256.1:n.1352+1G>A
NM_006254.3:c.1352+1G>A	NP_006245.2:n.1352+1G>A
NM_212539.1:c.1352+1G>A	NP_997704.1:n.1352+1G>A
XM_006713257.2:c.1400+1G>A	XP_006713320.1:n.1400+1G>A
XM_006713259.2:c.1352+1G>A	XP_006713322.1:n.1352+1G>A
XR_940474.1:n.1270+1G>A
NM_001354676.1:c.1409+1G>A	NP_001341605.1:n.1409+1G>A
NM_001354678.1:c.1400+1G>A	NP_001341607.1:n.1400+1G>A
NM_001354679.1:c.1352+1G>A	NP_001341608.1:n.1352+1G>A
NM_001354680.1:c.1352+1G>A	NP_001341609.1:n.1352+1G>A
XR_002959550.1:n.1323+1G>A
NM_006254.4:c.1352+1G>A MANE Select	NP_006245.2:n.1352+1G>A
NM_001316327.2:c.1352+1G>A	NP_001303256.1:n.1352+1G>A
NM_001354676.2:c.1409+1G>A	NP_001341605.1:n.1409+1G>A
NM_001354678.2:c.1400+1G>A	NP_001341607.1:n.1400+1G>A
NM_001354679.2:c.1352+1G>A	NP_001341608.1:n.1352+1G>A
NM_001354680.2:c.1352+1G>A	NP_001341609.1:n.1352+1G>A
NM_212539.2:c.1352+1G>A	NP_997704.1:n.1352+1G>A