Canonical Allele Identifier: CA2213524819

Gene: PRKCB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23877519T= , CM000678.2:g.23877519T=	GRCh38
NC_000016.9:g.23888840T= , CM000678.1:g.23888840T=	GRCh37
NC_000016.8:g.23796341T=	NCBI36
NG_029003.1:g.46541T=
NG_029003.2:g.46541T=

Transcript Alleles

HGVS	Amino-acid Change
NM_002738.7:c.205+40113T= MANE Select	NP_002729.2:n.205+40113T=
ENST00000643927.1:c.205+40113T= MANE Select	ENSP00000496129.1:n.205+40113T=
NM_002738.6:c.205+40113T=	NP_002729.2:n.205+40113T=
NM_212535.2:c.205+40113T=	NP_997700.1:n.205+40113T=
NM_212535.3:c.205+40113T=	NP_997700.1:n.205+40113T=
ENST00000303531.11:c.205+40113T=	ENSP00000305355.7:n.205+40113T=
ENST00000321728.11:c.205+40113T=	ENSP00000318315.7:n.205+40113T=
ENST00000321728.12:c.205+40113T=	ENSP00000318315.7:n.205+40113T=
ENST00000498739.1:c.-27+40113T=	ENSP00000459227.1:n.-27+40113T=
ENST00000645517.1:n.153-15445T=