Canonical Allele Identifier: CA2695197923

Gene: PRKCD

Linked Data

• ClinVar Variation Id: 2628232
• ClinVar RCV Id: RCV003397091
• dbSNP Id: rs2107257773

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53179808_53179809insGGTG , CM000665.2:g.53179808_53179809insGGTG	GRCh38
NC_000003.11:g.53213824_53213825insGGTG , CM000665.1:g.53213824_53213825insGGTG	GRCh37
NC_000003.10:g.53188864_53188865insGGTG	NCBI36
NG_033864.1:g.23602_23603insGGTG
NG_033864.2:g.28800_28801insGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697588.1:c.315+32_315+33insGGTG	ENSP00000513355.1:n.315+32_315+33insGGTG
ENST00000330452.8:c.315+32_315+33insGGTG MANE Select	ENSP00000331602.3:n.315+32_315+33insGGTG
ENST00000650739.1:c.315+32_315+33insGGTG	ENSP00000498623.1:n.315+32_315+33insGGTG
ENST00000650940.1:c.315+32_315+33insGGTG	ENSP00000499184.1:n.315+32_315+33insGGTG
ENST00000652449.1:c.315+32_315+33insGGTG	ENSP00000498400.1:n.315+32_315+33insGGTG
ENST00000654719.1:c.315+32_315+33insGGTG	ENSP00000499558.1:n.315+32_315+33insGGTG
ENST00000330452.7:c.315+32_315+33insGGTG	ENSP00000331602.3:n.315+32_315+33insGGTG
ENST00000394729.6:c.315+32_315+33insGGTG	ENSP00000378217.2:n.315+32_315+33insGGTG
ENST00000464818.1:c.315+32_315+33insGGTG	ENSP00000419629.1:n.315+32_315+33insGGTG
ENST00000487897.5:c.315+32_315+33insGGTG	ENSP00000418106.1:n.315+32_315+33insGGTG
NM_001316327.1:c.315+32_315+33insGGTG	NP_001303256.1:n.315+32_315+33insGGTG
NM_006254.3:c.315+32_315+33insGGTG	NP_006245.2:n.315+32_315+33insGGTG
NM_212539.1:c.315+32_315+33insGGTG	NP_997704.1:n.315+32_315+33insGGTG
XM_006713257.2:c.363+32_363+33insGGTG	XP_006713320.1:n.363+32_363+33insGGTG
XM_006713259.2:c.315+32_315+33insGGTG	XP_006713322.1:n.315+32_315+33insGGTG
XR_940474.1:n.334+32_334+33insGGTG
NM_001354676.1:c.372+32_372+33insGGTG	NP_001341605.1:n.372+32_372+33insGGTG
NM_001354678.1:c.363+32_363+33insGGTG	NP_001341607.1:n.363+32_363+33insGGTG
NM_001354679.1:c.315+32_315+33insGGTG	NP_001341608.1:n.315+32_315+33insGGTG
NM_001354680.1:c.315+32_315+33insGGTG	NP_001341609.1:n.315+32_315+33insGGTG
XR_002959550.1:n.387+32_387+33insGGTG
NM_006254.4:c.315+32_315+33insGGTG MANE Select	NP_006245.2:n.315+32_315+33insGGTG
NM_001316327.2:c.315+32_315+33insGGTG	NP_001303256.1:n.315+32_315+33insGGTG
NM_001354676.2:c.372+32_372+33insGGTG	NP_001341605.1:n.372+32_372+33insGGTG
NM_001354678.2:c.363+32_363+33insGGTG	NP_001341607.1:n.363+32_363+33insGGTG
NM_001354679.2:c.315+32_315+33insGGTG	NP_001341608.1:n.315+32_315+33insGGTG
NM_001354680.2:c.315+32_315+33insGGTG	NP_001341609.1:n.315+32_315+33insGGTG
NM_212539.2:c.315+32_315+33insGGTG	NP_997704.1:n.315+32_315+33insGGTG