Canonical Allele Identifier: CA353233856

Gene: PRKCD

Linked Data

• ClinVar Variation Id: 1358064
• ClinVar RCV Id: RCV001878535
• dbSNP Id: rs1553667410
• MyVariant Identifiers: chr3:g.53215283G>T (hg19) ; chr3:g.53181267G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53181267G>T , CM000665.2:g.53181267G>T	GRCh38
NC_000003.11:g.53215283G>T , CM000665.1:g.53215283G>T	GRCh37
NC_000003.10:g.53190323G>T	NCBI36
NG_033864.1:g.25061G>T
NG_033864.2:g.30259G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697588.1:c.376G>T	ENSP00000513355.1:p.Asp126Tyr
ENST00000330452.8:c.376G>T MANE Select	ENSP00000331602.3:p.Asp126Tyr
ENST00000650739.1:c.376G>T	ENSP00000498623.1:p.Asp126Tyr
ENST00000650940.1:c.376G>T	ENSP00000499184.1:p.Asp126Tyr
ENST00000651505.1:c.8G>T
ENST00000652449.1:c.376G>T	ENSP00000498400.1:p.Asp126Tyr
ENST00000654719.1:c.376G>T	ENSP00000499558.1:p.Asp126Tyr
ENST00000330452.7:c.376G>T	ENSP00000331602.3:p.Asp126Tyr
ENST00000394729.6:c.376G>T	ENSP00000378217.2:p.Asp126Tyr
ENST00000464818.1:c.376G>T	ENSP00000419629.1:p.Asp126Tyr
ENST00000487897.5:c.376G>T
NM_001316327.1:c.376G>T	NP_001303256.1:p.Asp126Tyr
NM_006254.3:c.376G>T	NP_006245.2:p.Asp126Tyr
NM_212539.1:c.376G>T	NP_997704.1:p.Asp126Tyr
XM_006713257.2:c.424G>T	XP_006713320.1:p.Asp142Tyr
XM_006713259.2:c.376G>T	XP_006713322.1:p.Asp126Tyr
XR_940474.1:n.395G>T
NM_001354676.1:c.433G>T	NP_001341605.1:p.Asp145Tyr
NM_001354678.1:c.424G>T	NP_001341607.1:p.Asp142Tyr
NM_001354679.1:c.376G>T	NP_001341608.1:p.Asp126Tyr
NM_001354680.1:c.376G>T	NP_001341609.1:p.Asp126Tyr
XR_002959550.1:n.448G>T
NM_006254.4:c.376G>T MANE Select	NP_006245.2:p.Asp126Tyr
NM_001316327.2:c.376G>T	NP_001303256.1:p.Asp126Tyr
NM_001354676.2:c.433G>T	NP_001341605.1:p.Asp145Tyr
NM_001354678.2:c.424G>T	NP_001341607.1:p.Asp142Tyr
NM_001354679.2:c.376G>T	NP_001341608.1:p.Asp126Tyr
NM_001354680.2:c.376G>T	NP_001341609.1:p.Asp126Tyr
NM_212539.2:c.376G>T	NP_997704.1:p.Asp126Tyr