Canonical Allele Identifier: CA2141255786

Gene: PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61441680C= , CM000676.2:g.61441680C=	GRCh38
NC_000014.8:g.61908398C= , CM000676.1:g.61908398C=	GRCh37
NC_000014.7:g.60978151C=	NCBI36
NG_011514.1:g.124884C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332981.11:c.428-1431C= MANE Select	ENSP00000329127.5:n.428-1431C=
ENST00000332981.10:c.428-1431C=	ENSP00000329127.5:n.428-1431C=
ENST00000332981.9:c.428-1431C=	ENSP00000329127.5:n.428-1431C=
ENST00000553265.5:c.-56-1431C=	ENSP00000451933.1:n.-56-1431C=
ENST00000553726.5:c.-229-4012C=	ENSP00000451793.1:n.-229-4012C=
ENST00000553830.1:c.254-1431C=	ENSP00000452588.1:n.254-1431C=
ENST00000553831.5:c.-56-1431C=	ENSP00000450959.1:n.-56-1431C=
ENST00000555082.5:c.-56-1431C=	ENSP00000450981.1:n.-56-1431C=
ENST00000555185.5:c.-18-43822C=	ENSP00000451871.1:n.-18-43822C=
ENST00000555542.5:c.-56-1431C=	ENSP00000451789.1:n.-56-1431C=
ENST00000555906.5:c.-56-1431C=	ENSP00000451205.1:n.-56-1431C=
ENST00000556164.5:c.-56-1431C=	ENSP00000452330.1:n.-56-1431C=
ENST00000556778.5:c.-56-1431C=	ENSP00000452055.1:n.-56-1431C=
ENST00000557585.5:c.-56-1431C=	ENSP00000451930.1:n.-56-1431C=
NM_006255.4:c.428-1431C=	NP_006246.2:n.428-1431C=
XM_011536954.1:c.191-1431C=	XP_011535256.1:n.191-1431C=
XM_011536955.1:c.188-1431C=	XP_011535257.1:n.188-1431C=
XM_011536956.1:c.428-1431C=	XP_011535258.1:n.428-1431C=
XM_011536957.1:c.428-1431C=	XP_011535259.1:n.428-1431C=
XM_011536954.3:c.191-1431C=	XP_011535256.1:n.191-1431C=
XM_017021458.1:c.-56-1431C=	XP_016876947.1:n.-56-1431C=
XM_017021459.1:c.428-1431C=	XP_016876948.1:n.428-1431C=
XM_024449661.1:c.-56-1431C=	XP_024305429.1:n.-56-1431C=
XM_024449662.1:c.-56-1431C=	XP_024305430.1:n.-56-1431C=
NM_006255.5:c.428-1431C= MANE Select	NP_006246.2:n.428-1431C=