Canonical Allele Identifier: CA632117114
Gene: PRKCSH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11447591_11447602del , CM000681.2:g.11447591_11447602del GRCh38
NC_000019.9:g.11558406_11558417del , CM000681.1:g.11558406_11558417del GRCh37
NC_000019.8:g.11419406_11419417del NCBI36
NG_009300.1:g.17138_17149del

Transcript Alleles

HGVS Amino-acid Change
ENST00000591462.6:c.1002_1013del ENSP00000465489.1:p.Asp334_Gln338delinsGlu
ENST00000677123.1:c.1002_1013del MANE Select ENSP00000503163.1:p.Asp334_Gln338delinsGlu
ENST00000585325.5:n.275_286del
ENST00000585540.1:n.193_204del
ENST00000586486.1:c.27_38del ENSP00000465948.1:p.Asp9_Gln13delinsGlu
ENST00000587327.5:c.1002_1013del ENSP00000466012.1:p.Asp334_Gln338delinsGlu
ENST00000589838.5:c.1002_1008+5del
ENST00000591462.5:c.1002_1013del ENSP00000465489.1:p.Asp334_Gln338delinsGlu
ENST00000592445.1:n.249_260del
ENST00000592741.5:c.1002_1013del ENSP00000466134.1:p.Asp334_Gln338delinsGlu
NM_001001329.2:c.1002_1013del NP_001001329.1:p.Asp334_Gln338delinsGlu
NM_001289102.1:c.1002_1013del NP_001276031.1:p.Asp334_Gln338delinsGlu
NM_001289103.1:c.1002_1013del NP_001276032.1:p.Asp334_Gln338delinsGlu
NM_001289104.1:c.1002_1013del NP_001276033.1:p.Asp334_Gln338delinsGlu
NM_002743.3:c.1002_1008+5del
XM_011528130.1:c.1002_1013del XP_011526432.1:p.Asp334_Gln338delinsGlu
XM_011528131.1:c.1002_1008+5del
XM_011528132.1:c.1002_1013del XP_011526434.1:p.Asp334_Gln338delinsGlu
XM_017026977.2:c.1002_1008+5del
XM_024451602.1:c.1002_1013del XP_024307370.1:p.Asp334_Gln338delinsGlu
NM_001001329.3:c.1002_1013del NP_001001329.1:p.Asp334_Gln338delinsGlu
NM_001289102.2:c.1002_1013del NP_001276031.1:p.Asp334_Gln338delinsGlu
NM_001289103.2:c.1002_1013del NP_001276032.1:p.Asp334_Gln338delinsGlu
NM_001289104.2:c.1002_1013del MANE Select NP_001276033.1:p.Asp334_Gln338delinsGlu
NM_001379608.1:c.1002_1008+5del
NM_001379609.1:c.1002_1013del NP_001366538.1:p.Asp334_Gln338delinsGlu