Canonical Allele Identifier: CA1888258805

Gene: PRKCQ

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6564579C= , CM000672.2:g.6564579C=	GRCh38
NC_000010.10:g.6606541C= , CM000672.1:g.6606541C=	GRCh37
NC_000010.9:g.6646547C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006257.5:c.-10+15632G= MANE Select	NP_006248.1:n.-10+15632G=
ENST00000263125.10:c.-10+15632G= MANE Select	ENSP00000263125.5:n.-10+15632G=
NM_001242413.2:c.-10+15632G=	NP_001229342.1:n.-10+15632G=
NM_001282644.1:c.-116+15632G=	NP_001269573.1:n.-116+15632G=
NM_001282644.2:c.-116+15632G=	NP_001269573.1:n.-116+15632G=
NM_001282645.1:c.-324+15632G=	NP_001269574.1:n.-324+15632G=
NM_001323265.1:c.-10+15922G=	NP_001310194.1:n.-10+15922G=
NM_001323266.1:c.-322+15632G=	NP_001310195.1:n.-322+15632G=
NM_001323266.2:c.-322+15632G=	NP_001310195.1:n.-322+15632G=
NM_001323267.1:c.-116+15632G=	NP_001310196.1:n.-116+15632G=
NM_001323267.2:c.-116+15632G=	NP_001310196.1:n.-116+15632G=
NM_006257.4:c.-10+15632G=	NP_006248.1:n.-10+15632G=
ENST00000263125.9:c.-10+15632G=	ENSP00000263125.5:n.-10+15632G=
ENST00000397176.6:c.-10+15632G=	ENSP00000380361.2:n.-10+15632G=
ENST00000539722.5:c.-324+15632G=	ENSP00000441752.1:n.-324+15632G=
XM_011519547.1:c.-10+15922G=	XP_011517849.1:n.-10+15922G=