Canonical Allele Identifier: CA2580603361
Gene: PRKCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.61452425C>A , CM000676.2:g.61452425C>A GRCh38
NC_000014.8:g.61919143C>A , CM000676.1:g.61919143C>A GRCh37
NC_000014.7:g.60988896C>A NCBI36
NG_011514.1:g.135629C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000332981.11:c.833-801C>A MANE Select ENSP00000329127.5:n.833-801C>A
ENST00000332981.10:c.833-801C>A ENSP00000329127.5:n.833-801C>A
ENST00000332981.9:c.833-801C>A ENSP00000329127.5:n.833-801C>A
ENST00000553726.5:c.26-801C>A ENSP00000451793.1:n.26-801C>A
ENST00000555082.5:c.350-801C>A ENSP00000450981.1:n.350-801C>A
ENST00000555185.5:c.-18-33077C>A ENSP00000451871.1:n.-18-33077C>A
ENST00000556778.5:c.350-801C>A ENSP00000452055.1:n.350-801C>A
ENST00000557585.5:c.350-801C>A ENSP00000451930.1:n.350-801C>A
NM_006255.4:c.833-801C>A NP_006246.2:n.833-801C>A
XM_011536954.1:c.596-801C>A XP_011535256.1:n.596-801C>A
XM_011536955.1:c.593-801C>A XP_011535257.1:n.593-801C>A
XM_011536956.1:c.833-801C>A XP_011535258.1:n.833-801C>A
XM_011536957.1:c.833-801C>A XP_011535259.1:n.833-801C>A
XM_011536954.3:c.596-801C>A XP_011535256.1:n.596-801C>A
XM_017021458.1:c.350-801C>A XP_016876947.1:n.350-801C>A
XM_017021459.1:c.833-801C>A XP_016876948.1:n.833-801C>A
XM_024449661.1:c.350-801C>A XP_024305429.1:n.350-801C>A
XM_024449662.1:c.350-801C>A XP_024305430.1:n.350-801C>A
NM_006255.5:c.833-801C>A MANE Select NP_006246.2:n.833-801C>A