Canonical Allele Identifier: CA2451705

Gene: PRKCD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53179675G>C , CM000665.2:g.53179675G>C	GRCh38
NC_000003.11:g.53213691G>C , CM000665.1:g.53213691G>C	GRCh37
NC_000003.10:g.53188731G>C	NCBI36
NG_033864.1:g.23469G>C
NG_033864.2:g.28667G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697588.1:c.214G>C	ENSP00000513355.1:p.Val72Leu
ENST00000330452.8:c.214G>C MANE Select	ENSP00000331602.3:p.Val72Leu
ENST00000650739.1:c.214G>C	ENSP00000498623.1:p.Val72Leu
ENST00000650940.1:c.214G>C	ENSP00000499184.1:p.Val72Leu
ENST00000652449.1:c.214G>C	ENSP00000498400.1:p.Val72Leu
ENST00000654719.1:c.214G>C	ENSP00000499558.1:p.Val72Leu
ENST00000330452.7:c.214G>C	ENSP00000331602.3:p.Val72Leu
ENST00000394729.6:c.214G>C	ENSP00000378217.2:p.Val72Leu
ENST00000464818.1:c.214G>C	ENSP00000419629.1:p.Val72Leu
ENST00000478843.5:c.214G>C	ENSP00000419726.1:p.Val72Leu
ENST00000487897.5:c.214G>C	ENSP00000418106.1:p.Val72Leu
NM_001316327.1:c.214G>C	NP_001303256.1:p.Val72Leu
NM_006254.3:c.214G>C	NP_006245.2:p.Val72Leu
NM_212539.1:c.214G>C	NP_997704.1:p.Val72Leu
XM_006713257.2:c.262G>C	XP_006713320.1:p.Val88Leu
XM_006713259.2:c.214G>C	XP_006713322.1:p.Val72Leu
XR_940474.1:n.233G>C
NM_001354676.1:c.271G>C	NP_001341605.1:p.Val91Leu
NM_001354678.1:c.262G>C	NP_001341607.1:p.Val88Leu
NM_001354679.1:c.214G>C	NP_001341608.1:p.Val72Leu
NM_001354680.1:c.214G>C	NP_001341609.1:p.Val72Leu
XR_002959550.1:n.286G>C
NM_006254.4:c.214G>C MANE Select	NP_006245.2:p.Val72Leu
NM_001316327.2:c.214G>C	NP_001303256.1:p.Val72Leu
NM_001354676.2:c.271G>C	NP_001341605.1:p.Val91Leu
NM_001354678.2:c.262G>C	NP_001341607.1:p.Val88Leu
NM_001354679.2:c.214G>C	NP_001341608.1:p.Val72Leu
NM_001354680.2:c.214G>C	NP_001341609.1:p.Val72Leu
NM_212539.2:c.214G>C	NP_997704.1:p.Val72Leu