Canonical Allele Identifier: CA389922687
Gene: PRKCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.61485580G>A , CM000676.2:g.61485580G>A GRCh38
NC_000014.8:g.61952298G>A , CM000676.1:g.61952298G>A GRCh37
NC_000014.7:g.61022051G>A NCBI36
NG_011514.1:g.168784G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332981.11:c.1357G>A MANE Select ENSP00000329127.5:p.Glu453Lys
ENST00000332981.10:c.1357G>A ENSP00000329127.5:p.Glu453Lys
ENST00000640011.1:c.46G>A ENSP00000491586.1:p.Glu16Lys
ENST00000332981.9:c.1357G>A ENSP00000329127.5:p.Glu453Lys
ENST00000536400.5:n.158G>A
ENST00000555082.5:c.874G>A ENSP00000450981.1:p.Glu292Lys
ENST00000555185.5:c.61G>A ENSP00000451871.1:p.Glu21Lys
ENST00000555233.5:n.371G>A
NM_006255.4:c.1357G>A NP_006246.2:p.Glu453Lys
XM_011536954.1:c.1120G>A XP_011535256.1:p.Glu374Lys
XM_011536955.1:c.1117G>A XP_011535257.1:p.Glu373Lys
XM_011536956.1:c.1357G>A XP_011535258.1:p.Glu453Lys
XM_011536957.1:c.1357G>A XP_011535259.1:p.Glu453Lys
XM_011536954.3:c.1120G>A XP_011535256.1:p.Glu374Lys
XM_017021458.1:c.874G>A XP_016876947.1:p.Glu292Lys
XM_024449661.1:c.874G>A XP_024305429.1:p.Glu292Lys
XM_024449662.1:c.874G>A XP_024305430.1:p.Glu292Lys
NM_006255.5:c.1357G>A MANE Select NP_006246.2:p.Glu453Lys