Canonical Allele Identifier: CA2451642

Gene: PRKCD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53178551C>G , CM000665.2:g.53178551C>G	GRCh38
NC_000003.11:g.53212567C>G , CM000665.1:g.53212567C>G	GRCh37
NC_000003.10:g.53187607C>G	NCBI36
NG_033864.1:g.22345C>G
NG_033864.2:g.27543C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006254.4:c.115+14C>G MANE Select	NP_006245.2:n.115+14C>G
ENST00000330452.8:c.115+14C>G MANE Select	ENSP00000331602.3:n.115+14C>G
NM_001316327.1:c.115+14C>G	NP_001303256.1:n.115+14C>G
NM_001316327.2:c.115+14C>G	NP_001303256.1:n.115+14C>G
NM_001354676.1:c.172+14C>G	NP_001341605.1:n.172+14C>G
NM_001354676.2:c.172+14C>G	NP_001341605.1:n.172+14C>G
NM_001354678.1:c.163+14C>G	NP_001341607.1:n.163+14C>G
NM_001354678.2:c.163+14C>G	NP_001341607.1:n.163+14C>G
NM_001354679.1:c.115+14C>G	NP_001341608.1:n.115+14C>G
NM_001354679.2:c.115+14C>G	NP_001341608.1:n.115+14C>G
NM_001354680.1:c.115+14C>G	NP_001341609.1:n.115+14C>G
NM_001354680.2:c.115+14C>G	NP_001341609.1:n.115+14C>G
NM_006254.3:c.115+14C>G	NP_006245.2:n.115+14C>G
NM_212539.1:c.115+14C>G	NP_997704.1:n.115+14C>G
NM_212539.2:c.115+14C>G	NP_997704.1:n.115+14C>G
ENST00000330452.7:c.115+14C>G	ENSP00000331602.3:n.115+14C>G
ENST00000394729.6:c.115+14C>G	ENSP00000378217.2:n.115+14C>G
ENST00000464818.1:c.115+14C>G	ENSP00000419629.1:n.115+14C>G
ENST00000478843.5:c.115+14C>G	ENSP00000419726.1:n.115+14C>G
ENST00000487897.5:c.115+14C>G	ENSP00000418106.1:n.115+14C>G
ENST00000650739.1:c.115+14C>G	ENSP00000498623.1:n.115+14C>G
ENST00000650940.1:c.115+14C>G	ENSP00000499184.1:n.115+14C>G
ENST00000652449.1:c.115+14C>G	ENSP00000498400.1:n.115+14C>G
ENST00000654719.1:c.115+14C>G	ENSP00000499558.1:n.115+14C>G
ENST00000697588.1:c.115+14C>G	ENSP00000513355.1:n.115+14C>G
XM_006713257.2:c.163+14C>G	XP_006713320.1:n.163+14C>G
XM_006713259.2:c.115+14C>G	XP_006713322.1:n.115+14C>G
XR_002959550.1:n.187+14C>G
XR_940474.1:n.134+14C>G