Canonical Allele Identifier: CA9213014
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 328184
dbSNP Id: rs139969239

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11447145C>T , CM000681.2:g.11447145C>T GRCh38
NC_000019.9:g.11557960C>T , CM000681.1:g.11557960C>T GRCh37
NC_000019.8:g.11418960C>T NCBI36
NG_009300.1:g.16692C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000591462.6:c.834C>T ENSP00000465489.1:p.Asp278=
ENST00000677123.1:c.834C>T MANE Select ENSP00000503163.1:p.Asp278=
ENST00000585325.5:n.107C>T
ENST00000585540.1:n.25C>T
ENST00000587327.5:c.834C>T ENSP00000466012.1:p.Asp278=
ENST00000589838.5:c.834C>T ENSP00000465461.1:p.Asp278=
ENST00000591462.5:c.834C>T ENSP00000465489.1:p.Asp278=
ENST00000592445.1:n.81C>T
ENST00000592741.5:c.834C>T ENSP00000466134.1:p.Asp278=
NM_001001329.2:c.834C>T NP_001001329.1:p.Asp278=
NM_001289102.1:c.834C>T NP_001276031.1:p.Asp278=
NM_001289103.1:c.834C>T NP_001276032.1:p.Asp278=
NM_001289104.1:c.834C>T NP_001276033.1:p.Asp278=
NM_002743.3:c.834C>T NP_002734.2:p.Asp278=
XM_011528130.1:c.834C>T XP_011526432.1:p.Asp278=
XM_011528131.1:c.834C>T XP_011526433.1:p.Asp278=
XM_011528132.1:c.834C>T XP_011526434.1:p.Asp278=
XM_017026977.2:c.834C>T XP_016882466.1:p.Asp278=
XM_024451602.1:c.834C>T XP_024307370.1:p.Asp278=
NM_001001329.3:c.834C>T NP_001001329.1:p.Asp278=
NM_001289102.2:c.834C>T NP_001276031.1:p.Asp278=
NM_001289103.2:c.834C>T NP_001276032.1:p.Asp278=
NM_001289104.2:c.834C>T MANE Select NP_001276033.1:p.Asp278=
NM_001379608.1:c.834C>T NP_001366537.1:p.Asp278=
NM_001379609.1:c.834C>T NP_001366538.1:p.Asp278=