Canonical Allele Identifier: CA2322940073
Gene: PRKCSH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11447113_11447154delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG , CM000681.2:g.11447113_11447154delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG GRCh38
NC_000019.9:g.11557928_11557969delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG , CM000681.1:g.11557928_11557969delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG GRCh37
NC_000019.8:g.11418928_11418969delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NCBI36
NG_009300.1:g.16660_16701delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000591462.6:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG ENSP00000465489.1:p.Phe268=
ENST00000677123.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG MANE Select ENSP00000503163.1:p.Phe268=
ENST00000585325.5:n.75_116delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG
ENST00000587327.5:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG ENSP00000466012.1:p.Phe268=
ENST00000589838.5:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG ENSP00000465461.1:p.Phe268=
ENST00000591462.5:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG ENSP00000465489.1:p.Phe268=
ENST00000592445.1:n.49_90delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG
ENST00000592741.5:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG ENSP00000466134.1:p.Phe268=
NM_001001329.2:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_001001329.1:p.Phe268=
NM_001289102.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_001276031.1:p.Phe268=
NM_001289103.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_001276032.1:p.Phe268=
NM_001289104.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_001276033.1:p.Phe268=
NM_002743.3:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_002734.2:p.Phe268=
XM_011528130.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG XP_011526432.1:p.Phe268=
XM_011528131.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG XP_011526433.1:p.Phe268=
XM_011528132.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG XP_011526434.1:p.Phe268=
XM_017026977.2:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG XP_016882466.1:p.Phe268=
XM_024451602.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG XP_024307370.1:p.Phe268=
NM_001001329.3:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_001001329.1:p.Phe268=
NM_001289102.2:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_001276031.1:p.Phe268=
NM_001289103.2:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_001276032.1:p.Phe268=
NM_001289104.2:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG MANE Select NP_001276033.1:p.Phe268=
NM_001379608.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_001366537.1:p.Phe268=
NM_001379609.1:c.802_843delinsTTCTACGACCGCGTCTGGGCCGCCATCAGGGACAAGTACCGG NP_001366538.1:p.Phe268=