Canonical Allele Identifier: CA7215304

Gene: PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61457519G>C , CM000676.2:g.61457519G>C	GRCh38
NC_000014.8:g.61924237G>C , CM000676.1:g.61924237G>C	GRCh37
NC_000014.7:g.60993990G>C	NCBI36
NG_011514.1:g.140723G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332981.11:c.1118G>C MANE Select	ENSP00000329127.5:p.Arg373Thr
ENST00000332981.10:c.1118G>C	ENSP00000329127.5:p.Arg373Thr
ENST00000332981.9:c.1118G>C	ENSP00000329127.5:p.Arg373Thr
ENST00000553889.5:n.419G>C
ENST00000555082.5:c.635G>C	ENSP00000450981.1:p.Arg212Thr
ENST00000555185.5:c.-18-27983G>C	ENSP00000451871.1:n.-18-27983G>C
ENST00000555604.1:n.14G>C
ENST00000557559.1:n.398G>C
ENST00000557585.5:c.635G>C	ENSP00000451930.1:p.Arg212Thr
NM_006255.4:c.1118G>C	NP_006246.2:p.Arg373Thr
XM_011536954.1:c.881G>C	XP_011535256.1:p.Arg294Thr
XM_011536955.1:c.878G>C	XP_011535257.1:p.Arg293Thr
XM_011536956.1:c.1118G>C	XP_011535258.1:p.Arg373Thr
XM_011536957.1:c.1118G>C	XP_011535259.1:p.Arg373Thr
XM_011536954.3:c.881G>C	XP_011535256.1:p.Arg294Thr
XM_017021458.1:c.635G>C	XP_016876947.1:p.Arg212Thr
XM_017021459.1:c.1118G>C	XP_016876948.1:p.Arg373Thr
XM_024449661.1:c.635G>C	XP_024305429.1:p.Arg212Thr
XM_024449662.1:c.635G>C	XP_024305430.1:p.Arg212Thr
NM_006255.5:c.1118G>C MANE Select	NP_006246.2:p.Arg373Thr