Canonical Allele Identifier: CA433796184
Gene: PRKCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2792901
ClinVar RCV Id: RCV003745814
dbSNP Id: rs1703822778
gnomAD v4: 3-53189072-G-A
MyVariant Identifiers: chr3:g.53223088G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53189072G>A , CM000665.2:g.53189072G>A GRCh38
NC_000003.11:g.53223088G>A , CM000665.1:g.53223088G>A GRCh37
NC_000003.10:g.53198128G>A NCBI36
NG_033864.1:g.32866G>A
NG_033864.2:g.38064G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697588.1:c.*397G>A ENSP00000513355.1:n.*397G>A
ENST00000697589.1:n.1573G>A
ENST00000697590.1:n.568G>A
ENST00000330452.8:c.1569G>A MANE Select ENSP00000331602.3:p.Leu523=
ENST00000650739.1:c.1569G>A ENSP00000498623.1:p.Leu523=
ENST00000651505.1:c.1310G>A
ENST00000652449.1:c.1569G>A ENSP00000498400.1:p.Leu523=
ENST00000654719.1:c.1569G>A ENSP00000499558.1:p.Leu523=
ENST00000330452.7:c.1569G>A ENSP00000331602.3:p.Leu523=
ENST00000394729.6:c.1569G>A ENSP00000378217.2:p.Leu523=
NM_001316327.1:c.1569G>A NP_001303256.1:p.Leu523=
NM_006254.3:c.1569G>A NP_006245.2:p.Leu523=
NM_212539.1:c.1569G>A NP_997704.1:p.Leu523=
XM_006713257.2:c.1617G>A XP_006713320.1:p.Leu539=
XM_006713259.2:c.1569G>A XP_006713322.1:p.Leu523=
XR_940474.1:n.1487G>A
NM_001354676.1:c.1626G>A NP_001341605.1:p.Leu542=
NM_001354678.1:c.1617G>A NP_001341607.1:p.Leu539=
NM_001354679.1:c.1569G>A NP_001341608.1:p.Leu523=
NM_001354680.1:c.1569G>A NP_001341609.1:p.Leu523=
XR_002959550.1:n.1540G>A
NM_006254.4:c.1569G>A MANE Select NP_006245.2:p.Leu523=
NM_001316327.2:c.1569G>A NP_001303256.1:p.Leu523=
NM_001354676.2:c.1626G>A NP_001341605.1:p.Leu542=
NM_001354678.2:c.1617G>A NP_001341607.1:p.Leu539=
NM_001354679.2:c.1569G>A NP_001341608.1:p.Leu523=
NM_001354680.2:c.1569G>A NP_001341609.1:p.Leu523=
NM_212539.2:c.1569G>A NP_997704.1:p.Leu523=