Canonical Allele Identifier: CA2271288878

Gene: PRKCA

Linked Data

• dbSNP Id: rs1913779718

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66441816T>C , CM000679.2:g.66441816T>C	GRCh38
NC_000017.10:g.64437934T>C , CM000679.1:g.64437934T>C	GRCh37
NC_000017.9:g.61868396T>C	NCBI36
NG_012206.1:g.144009T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.206-54385T>C MANE Select	ENSP00000408695.3:n.206-54385T>C
ENST00000284384.6:c.198-54385T>C
ENST00000413366.7:c.206-54385T>C	ENSP00000408695.3:n.206-54385T>C
ENST00000578063.5:c.206-54385T>C	ENSP00000462087.1:n.206-54385T>C
NM_002737.2:c.206-54385T>C	NP_002728.1:n.206-54385T>C
XM_011524990.1:c.206-54385T>C	XP_011523292.1:n.206-54385T>C
XM_011524991.1:c.206-54385T>C	XP_011523293.1:n.206-54385T>C
XM_011524992.1:c.206-54385T>C	XP_011523294.1:n.206-54385T>C
XM_017024836.2:c.206-54385T>C	XP_016880325.1:n.206-54385T>C
XM_017024841.1:c.206-54385T>C	XP_016880330.1:n.206-54385T>C
XR_001752558.1:n.418-54385T>C
NM_002737.3:c.206-54385T>C MANE Select	NP_002728.2:n.206-54385T>C