Canonical Allele Identifier: CA2141292002

Gene: PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61473957G= , CM000676.2:g.61473957G=	GRCh38
NC_000014.8:g.61940675G= , CM000676.1:g.61940675G=	GRCh37
NC_000014.7:g.61010428G=	NCBI36
NG_011514.1:g.157161G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006255.5:c.1279-11545G= MANE Select	NP_006246.2:n.1279-11545G=
ENST00000332981.11:c.1279-11545G= MANE Select	ENSP00000329127.5:n.1279-11545G=
NM_006255.4:c.1279-11545G=	NP_006246.2:n.1279-11545G=
ENST00000332981.10:c.1279-11545G=	ENSP00000329127.5:n.1279-11545G=
ENST00000332981.9:c.1279-11545G=	ENSP00000329127.5:n.1279-11545G=
ENST00000555082.5:c.796-11545G=	ENSP00000450981.1:n.796-11545G=
ENST00000555185.5:c.-18-11545G=	ENSP00000451871.1:n.-18-11545G=
ENST00000555233.5:n.292+10597G=
ENST00000555604.1:n.175-2373G=
XM_011536954.1:c.1042-11545G=	XP_011535256.1:n.1042-11545G=
XM_011536954.3:c.1042-11545G=	XP_011535256.1:n.1042-11545G=
XM_011536955.1:c.1039-11545G=	XP_011535257.1:n.1039-11545G=
XM_011536956.1:c.1279-11545G=	XP_011535258.1:n.1279-11545G=
XM_011536957.1:c.1279-11545G=	XP_011535259.1:n.1279-11545G=
XM_017021458.1:c.796-11545G=	XP_016876947.1:n.796-11545G=
XM_024449661.1:c.796-11545G=	XP_024305429.1:n.796-11545G=
XM_024449662.1:c.796-11545G=	XP_024305430.1:n.796-11545G=