Canonical Allele Identifier: CA2271288850

Gene: PRKCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66441739_66441740delinsCT , CM000679.2:g.66441739_66441740delinsCT	GRCh38
NC_000017.10:g.64437857_64437858delinsCT , CM000679.1:g.64437857_64437858delinsCT	GRCh37
NC_000017.9:g.61868319_61868320delinsCT	NCBI36
NG_012206.1:g.143932_143933delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.206-54462_206-54461delinsCT MANE Select	ENSP00000408695.3:n.206-54462_206-54461delinsCT
ENST00000284384.6:c.198-54462_198-54461delinsCT
ENST00000413366.7:c.206-54462_206-54461delinsCT	ENSP00000408695.3:n.206-54462_206-54461delinsCT
ENST00000578063.5:c.206-54462_206-54461delinsCT	ENSP00000462087.1:n.206-54462_206-54461delinsCT
NM_002737.2:c.206-54462_206-54461delinsCT	NP_002728.1:n.206-54462_206-54461delinsCT
XM_011524990.1:c.206-54462_206-54461delinsCT	XP_011523292.1:n.206-54462_206-54461delinsCT
XM_011524991.1:c.206-54462_206-54461delinsCT	XP_011523293.1:n.206-54462_206-54461delinsCT
XM_011524992.1:c.206-54462_206-54461delinsCT	XP_011523294.1:n.206-54462_206-54461delinsCT
XM_017024836.2:c.206-54462_206-54461delinsCT	XP_016880325.1:n.206-54462_206-54461delinsCT
XM_017024841.1:c.206-54462_206-54461delinsCT	XP_016880330.1:n.206-54462_206-54461delinsCT
XR_001752558.1:n.418-54462_418-54461delinsCT
NM_002737.3:c.206-54462_206-54461delinsCT MANE Select	NP_002728.2:n.206-54462_206-54461delinsCT