Canonical Allele Identifier: CA14296109

Gene: PRKCB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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