Canonical Allele Identifier: CA2141269660

Gene: PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61452453G= , CM000676.2:g.61452453G=	GRCh38
NC_000014.8:g.61919171G= , CM000676.1:g.61919171G=	GRCh37
NC_000014.7:g.60988924G=	NCBI36
NG_011514.1:g.135657G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332981.11:c.833-773G= MANE Select	ENSP00000329127.5:n.833-773G=
ENST00000332981.10:c.833-773G=	ENSP00000329127.5:n.833-773G=
ENST00000332981.9:c.833-773G=	ENSP00000329127.5:n.833-773G=
ENST00000553726.5:c.26-773G=	ENSP00000451793.1:n.26-773G=
ENST00000555082.5:c.350-773G=	ENSP00000450981.1:n.350-773G=
ENST00000555185.5:c.-18-33049G=	ENSP00000451871.1:n.-18-33049G=
ENST00000556778.5:c.350-773G=	ENSP00000452055.1:n.350-773G=
ENST00000557585.5:c.350-773G=	ENSP00000451930.1:n.350-773G=
NM_006255.4:c.833-773G=	NP_006246.2:n.833-773G=
XM_011536954.1:c.596-773G=	XP_011535256.1:n.596-773G=
XM_011536955.1:c.593-773G=	XP_011535257.1:n.593-773G=
XM_011536956.1:c.833-773G=	XP_011535258.1:n.833-773G=
XM_011536957.1:c.833-773G=	XP_011535259.1:n.833-773G=
XM_011536954.3:c.596-773G=	XP_011535256.1:n.596-773G=
XM_017021458.1:c.350-773G=	XP_016876947.1:n.350-773G=
XM_017021459.1:c.833-773G=	XP_016876948.1:n.833-773G=
XM_024449661.1:c.350-773G=	XP_024305429.1:n.350-773G=
XM_024449662.1:c.350-773G=	XP_024305430.1:n.350-773G=
NM_006255.5:c.833-773G= MANE Select	NP_006246.2:n.833-773G=