Canonical Allele Identifier: CA9212821
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 328171
dbSNP Id: rs76485217

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11441235C>T , CM000681.2:g.11441235C>T GRCh38
NC_000019.9:g.11552050C>T , CM000681.1:g.11552050C>T GRCh37
NC_000019.8:g.11413050C>T NCBI36
NG_009300.1:g.10782C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000591462.6:c.351-5C>T ENSP00000465489.1:n.351-5C>T
ENST00000676823.1:c.351-5C>T ENSP00000503072.1:n.351-5C>T
ENST00000677123.1:c.351-5C>T MANE Select ENSP00000503163.1:n.351-5C>T
ENST00000587327.5:c.351-5C>T ENSP00000466012.1:n.351-5C>T
ENST00000587509.5:c.351-5C>T ENSP00000465821.1:n.351-5C>T
ENST00000589126.5:c.351-5C>T ENSP00000467566.1:n.351-5C>T
ENST00000589838.5:c.351-5C>T ENSP00000465461.1:n.351-5C>T
ENST00000591462.5:c.351-5C>T ENSP00000465489.1:n.351-5C>T
ENST00000592741.5:c.351-5C>T ENSP00000466134.1:n.351-5C>T
ENST00000593053.1:n.576-5C>T
ENST00000593101.5:c.351-5C>T ENSP00000465047.1:n.351-5C>T
NM_001001329.2:c.351-5C>T NP_001001329.1:n.351-5C>T
NM_001289102.1:c.351-5C>T NP_001276031.1:n.351-5C>T
NM_001289103.1:c.351-5C>T NP_001276032.1:n.351-5C>T
NM_001289104.1:c.351-5C>T NP_001276033.1:n.351-5C>T
NM_002743.3:c.351-5C>T NP_002734.2:n.351-5C>T
XM_011528130.1:c.351-5C>T XP_011526432.1:n.351-5C>T
XM_011528131.1:c.351-5C>T XP_011526433.1:n.351-5C>T
XM_011528132.1:c.351-5C>T XP_011526434.1:n.351-5C>T
XM_017026977.2:c.351-5C>T XP_016882466.1:n.351-5C>T
XM_024451602.1:c.351-5C>T XP_024307370.1:n.351-5C>T
NM_001001329.3:c.351-5C>T NP_001001329.1:n.351-5C>T
NM_001289102.2:c.351-5C>T NP_001276031.1:n.351-5C>T
NM_001289103.2:c.351-5C>T NP_001276032.1:n.351-5C>T
NM_001289104.2:c.351-5C>T MANE Select NP_001276033.1:n.351-5C>T
NM_001379608.1:c.351-5C>T NP_001366537.1:n.351-5C>T
NM_001379609.1:c.351-5C>T NP_001366538.1:n.351-5C>T