Canonical Allele Identifier: CA353220292

Gene: PRKCD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53184873G>T , CM000665.2:g.53184873G>T	GRCh38
NC_000003.11:g.53218889G>T , CM000665.1:g.53218889G>T	GRCh37
NC_000003.10:g.53193929G>T	NCBI36
NG_033864.1:g.28667G>T
NG_033864.2:g.33865G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006254.4:c.788-1G>T MANE Select	NP_006245.2:n.788-1G>T
ENST00000330452.8:c.788-1G>T MANE Select	ENSP00000331602.3:n.788-1G>T
NM_001316327.1:c.788-1G>T	NP_001303256.1:n.788-1G>T
NM_001316327.2:c.788-1G>T	NP_001303256.1:n.788-1G>T
NM_001354676.1:c.845-1G>T	NP_001341605.1:n.845-1G>T
NM_001354676.2:c.845-1G>T	NP_001341605.1:n.845-1G>T
NM_001354678.1:c.836-1G>T	NP_001341607.1:n.836-1G>T
NM_001354678.2:c.836-1G>T	NP_001341607.1:n.836-1G>T
NM_001354679.1:c.788-1G>T	NP_001341608.1:n.788-1G>T
NM_001354679.2:c.788-1G>T	NP_001341608.1:n.788-1G>T
NM_001354680.1:c.788-1G>T	NP_001341609.1:n.788-1G>T
NM_001354680.2:c.788-1G>T	NP_001341609.1:n.788-1G>T
NM_006254.3:c.788-1G>T	NP_006245.2:n.788-1G>T
NM_212539.1:c.788-1G>T	NP_997704.1:n.788-1G>T
NM_212539.2:c.788-1G>T	NP_997704.1:n.788-1G>T
ENST00000330452.7:c.788-1G>T	ENSP00000331602.3:n.788-1G>T
ENST00000394729.6:c.788-1G>T	ENSP00000378217.2:n.788-1G>T
ENST00000464818.1:c.572-1G>T	ENSP00000419629.1:n.572-1G>T
ENST00000650739.1:c.788-1G>T	ENSP00000498623.1:n.788-1G>T
ENST00000650940.1:c.788-1G>T	ENSP00000499184.1:n.788-1G>T
ENST00000651505.1:c.529-1G>T
ENST00000652449.1:c.788-1G>T	ENSP00000498400.1:n.788-1G>T
ENST00000654719.1:c.788-1G>T	ENSP00000499558.1:n.788-1G>T
ENST00000697588.1:c.788-1G>T	ENSP00000513355.1:n.788-1G>T
ENST00000697589.1:n.792-1G>T
XM_006713257.2:c.836-1G>T	XP_006713320.1:n.836-1G>T
XM_006713259.2:c.788-1G>T	XP_006713322.1:n.788-1G>T
XR_002959550.1:n.860-1G>T
XR_940474.1:n.807-1G>T