Canonical Allele Identifier: CA389917614

Gene: PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61457274C>G , CM000676.2:g.61457274C>G	GRCh38
NC_000014.8:g.61923992C>G , CM000676.1:g.61923992C>G	GRCh37
NC_000014.7:g.60993745C>G	NCBI36
NG_011514.1:g.140478C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332981.11:c.1059C>G MANE Select	ENSP00000329127.5:p.Asp353Glu
ENST00000332981.10:c.1059C>G	ENSP00000329127.5:p.Asp353Glu
ENST00000332981.9:c.1059C>G	ENSP00000329127.5:p.Asp353Glu
ENST00000553889.5:n.360C>G
ENST00000555082.5:c.576C>G	ENSP00000450981.1:p.Asp192Glu
ENST00000555185.5:c.-18-28228C>G	ENSP00000451871.1:n.-18-28228C>G
ENST00000557559.1:n.339C>G
ENST00000557585.5:c.576C>G	ENSP00000451930.1:p.Asp192Glu
NM_006255.4:c.1059C>G	NP_006246.2:p.Asp353Glu
XM_011536954.1:c.822C>G	XP_011535256.1:p.Asp274Glu
XM_011536955.1:c.819C>G	XP_011535257.1:p.Asp273Glu
XM_011536956.1:c.1059C>G	XP_011535258.1:p.Asp353Glu
XM_011536957.1:c.1059C>G	XP_011535259.1:p.Asp353Glu
XM_011536954.3:c.822C>G	XP_011535256.1:p.Asp274Glu
XM_017021458.1:c.576C>G	XP_016876947.1:p.Asp192Glu
XM_017021459.1:c.1059C>G	XP_016876948.1:p.Asp353Glu
XM_024449661.1:c.576C>G	XP_024305429.1:p.Asp192Glu
XM_024449662.1:c.576C>G	XP_024305430.1:p.Asp192Glu
NM_006255.5:c.1059C>G MANE Select	NP_006246.2:p.Asp353Glu