Canonical Allele Identifier: CA2141269640
Gene: PRKCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.61452440T= , CM000676.2:g.61452440T= GRCh38
NC_000014.8:g.61919158T= , CM000676.1:g.61919158T= GRCh37
NC_000014.7:g.60988911T= NCBI36
NG_011514.1:g.135644T=

Transcript Alleles

HGVS Amino-acid change
ENST00000332981.11:c.833-786T= MANE Select ENSP00000329127.5:n.833-786T=
ENST00000332981.10:c.833-786T= ENSP00000329127.5:n.833-786T=
ENST00000332981.9:c.833-786T= ENSP00000329127.5:n.833-786T=
ENST00000553726.5:c.26-786T= ENSP00000451793.1:n.26-786T=
ENST00000555082.5:c.350-786T= ENSP00000450981.1:n.350-786T=
ENST00000555185.5:c.-18-33062T= ENSP00000451871.1:n.-18-33062T=
ENST00000556778.5:c.350-786T= ENSP00000452055.1:n.350-786T=
ENST00000557585.5:c.350-786T= ENSP00000451930.1:n.350-786T=
NM_006255.4:c.833-786T= NP_006246.2:n.833-786T=
XM_011536954.1:c.596-786T= XP_011535256.1:n.596-786T=
XM_011536955.1:c.593-786T= XP_011535257.1:n.593-786T=
XM_011536956.1:c.833-786T= XP_011535258.1:n.833-786T=
XM_011536957.1:c.833-786T= XP_011535259.1:n.833-786T=
XM_011536954.3:c.596-786T= XP_011535256.1:n.596-786T=
XM_017021458.1:c.350-786T= XP_016876947.1:n.350-786T=
XM_017021459.1:c.833-786T= XP_016876948.1:n.833-786T=
XM_024449661.1:c.350-786T= XP_024305429.1:n.350-786T=
XM_024449662.1:c.350-786T= XP_024305430.1:n.350-786T=
NM_006255.5:c.833-786T= MANE Select NP_006246.2:n.833-786T=