Canonical Allele Identifier: CA2141277792

Gene: PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61457521G= , CM000676.2:g.61457521G=	GRCh38
NC_000014.8:g.61924239G= , CM000676.1:g.61924239G=	GRCh37
NC_000014.7:g.60993992G=	NCBI36
NG_011514.1:g.140725G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006255.5:c.1120G= MANE Select	NP_006246.2:p.Val374=
ENST00000332981.11:c.1120G= MANE Select	ENSP00000329127.5:p.Val374=
NM_006255.4:c.1120G=	NP_006246.2:p.Val374=
ENST00000332981.10:c.1120G=	ENSP00000329127.5:p.Val374=
ENST00000332981.9:c.1120G=	ENSP00000329127.5:p.Val374=
ENST00000553889.5:n.421G=
ENST00000555082.5:c.637G=	ENSP00000450981.1:p.Val213=
ENST00000555185.5:c.-18-27981G=	ENSP00000451871.1:n.-18-27981G=
ENST00000555604.1:n.16G=
ENST00000557559.1:n.400G=
ENST00000557585.5:c.637G=	ENSP00000451930.1:p.Val213=
XM_011536954.1:c.883G=	XP_011535256.1:p.Val295=
XM_011536954.3:c.883G=	XP_011535256.1:p.Val295=
XM_011536955.1:c.880G=	XP_011535257.1:p.Val294=
XM_011536956.1:c.1120G=	XP_011535258.1:p.Val374=
XM_011536957.1:c.1120G=	XP_011535259.1:p.Val374=
XM_017021458.1:c.637G=	XP_016876947.1:p.Val213=
XM_017021459.1:c.1120G=	XP_016876948.1:p.Val374=
XM_024449661.1:c.637G=	XP_024305429.1:p.Val213=
XM_024449662.1:c.637G=	XP_024305430.1:p.Val213=