Canonical Allele Identifier: CA7215023

Gene: PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61322429C>T , CM000676.2:g.61322429C>T	GRCh38
NC_000014.8:g.61789147C>T , CM000676.1:g.61789147C>T	GRCh37
NC_000014.7:g.60858900C>T	NCBI36
NG_011514.1:g.5633C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332981.11:c.328C>T MANE Select	ENSP00000329127.5:p.Arg110Cys
ENST00000332981.10:c.328C>T	ENSP00000329127.5:p.Arg110Cys
ENST00000332981.9:c.328C>T	ENSP00000329127.5:p.Arg110Cys
ENST00000555185.5:c.-19+134761C>T	ENSP00000451871.1:n.-19+134761C>T
ENST00000555542.5:c.-121+41121C>T	ENSP00000451789.1:n.-121+41121C>T
ENST00000555906.5:c.-121+41161C>T	ENSP00000451205.1:n.-121+41161C>T
ENST00000556778.5:c.-56-120682C>T	ENSP00000452055.1:n.-56-120682C>T
ENST00000557294.5:c.328C>T	ENSP00000452129.1:p.Arg110Cys
NM_006255.4:c.328C>T	NP_006246.2:p.Arg110Cys
XM_011536956.1:c.328C>T	XP_011535258.1:p.Arg110Cys
XM_011536957.1:c.328C>T	XP_011535259.1:p.Arg110Cys
XM_017021458.1:c.-121+41121C>T	XP_016876947.1:n.-121+41121C>T
XM_017021459.1:c.328C>T	XP_016876948.1:p.Arg110Cys
XM_024449661.1:c.-120-68796C>T	XP_024305429.1:n.-120-68796C>T
NM_006255.5:c.328C>T MANE Select	NP_006246.2:p.Arg110Cys