Canonical Allele Identifier: CA2838413940

Gene: PRKCB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23865045T>G , CM000678.2:g.23865045T>G	GRCh38
NC_000016.9:g.23876366T>G , CM000678.1:g.23876366T>G	GRCh37
NC_000016.8:g.23783867T>G	NCBI36
NG_029003.1:g.34067T>G
NG_029003.2:g.34067T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321728.12:c.205+27639T>G	ENSP00000318315.7:n.205+27639T>G
ENST00000643927.1:c.205+27639T>G MANE Select	ENSP00000496129.1:n.205+27639T>G
ENST00000645517.1:n.152+27639T>G
ENST00000303531.11:c.205+27639T>G	ENSP00000305355.7:n.205+27639T>G
ENST00000321728.11:c.205+27639T>G	ENSP00000318315.7:n.205+27639T>G
ENST00000498058.1:c.174-4069T>G	ENSP00000454428.1:n.174-4069T>G
ENST00000498739.1:c.-27+27639T>G	ENSP00000459227.1:n.-27+27639T>G
NM_002738.6:c.205+27639T>G	NP_002729.2:n.205+27639T>G
NM_212535.2:c.205+27639T>G	NP_997700.1:n.205+27639T>G
NM_002738.7:c.205+27639T>G MANE Select	NP_002729.2:n.205+27639T>G
NM_212535.3:c.205+27639T>G	NP_997700.1:n.205+27639T>G