Canonical Allele Identifier: CA1365206873

Gene: PRKCD

Linked Data

• ClinVar Variation Id: 2812387
• ClinVar RCV Id: RCV003744080
• dbSNP Id: rs1703943861

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53192088C>T , CM000665.2:g.53192088C>T	GRCh38
NC_000003.11:g.53226104C>T , CM000665.1:g.53226104C>T	GRCh37
NC_000003.10:g.53201144C>T	NCBI36
NG_033864.1:g.35882C>T
NG_033864.2:g.41080C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697588.1:c.*701-20C>T	ENSP00000513355.1:n.*701-20C>T
ENST00000697589.1:n.1877-20C>T
ENST00000697590.1:n.872-20C>T
ENST00000330452.8:c.1873-20C>T MANE Select	ENSP00000331602.3:n.1873-20C>T
ENST00000650739.1:c.1873-20C>T	ENSP00000498623.1:n.1873-20C>T
ENST00000651505.1:c.1614-20C>T
ENST00000652449.1:c.1873-20C>T	ENSP00000498400.1:n.1873-20C>T
ENST00000654719.1:c.1873-20C>T	ENSP00000499558.1:n.1873-20C>T
ENST00000330452.7:c.1873-20C>T	ENSP00000331602.3:n.1873-20C>T
ENST00000394729.6:c.1873-20C>T	ENSP00000378217.2:n.1873-20C>T
NM_001316327.1:c.1873-20C>T	NP_001303256.1:n.1873-20C>T
NM_006254.3:c.1873-20C>T	NP_006245.2:n.1873-20C>T
NM_212539.1:c.1873-20C>T	NP_997704.1:n.1873-20C>T
XM_006713257.2:c.1921-20C>T	XP_006713320.1:n.1921-20C>T
XM_006713259.2:c.1873-20C>T	XP_006713322.1:n.1873-20C>T
XR_940474.1:n.1791-20C>T
NM_001354676.1:c.1930-20C>T	NP_001341605.1:n.1930-20C>T
NM_001354678.1:c.1921-20C>T	NP_001341607.1:n.1921-20C>T
NM_001354679.1:c.1873-20C>T	NP_001341608.1:n.1873-20C>T
NM_001354680.1:c.1873-20C>T	NP_001341609.1:n.1873-20C>T
XR_002959550.1:n.1844-20C>T
NM_006254.4:c.1873-20C>T MANE Select	NP_006245.2:n.1873-20C>T
NM_001316327.2:c.1873-20C>T	NP_001303256.1:n.1873-20C>T
NM_001354676.2:c.1930-20C>T	NP_001341605.1:n.1930-20C>T
NM_001354678.2:c.1921-20C>T	NP_001341607.1:n.1921-20C>T
NM_001354679.2:c.1873-20C>T	NP_001341608.1:n.1873-20C>T
NM_001354680.2:c.1873-20C>T	NP_001341609.1:n.1873-20C>T
NM_212539.2:c.1873-20C>T	NP_997704.1:n.1873-20C>T