Canonical Allele Identifier: CA15906529

Gene: PRKCA

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66451047G>A , CM000679.2:g.66451047G>A	GRCh38
NC_000017.10:g.64447165G>A , CM000679.1:g.64447165G>A	GRCh37
NC_000017.9:g.61877627G>A	NCBI36
NG_012206.1:g.153240G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413366.8:c.206-45154G>A MANE Select	ENSP00000408695.3:n.206-45154G>A
ENST00000284384.6:c.198-45154G>A
ENST00000413366.7:c.206-45154G>A	ENSP00000408695.3:n.206-45154G>A
ENST00000578063.5:c.206-45154G>A	ENSP00000462087.1:n.206-45154G>A
NM_002737.2:c.206-45154G>A	NP_002728.1:n.206-45154G>A
XM_011524990.1:c.206-45154G>A	XP_011523292.1:n.206-45154G>A
XM_011524991.1:c.206-45154G>A	XP_011523293.1:n.206-45154G>A
XM_011524992.1:c.206-45154G>A	XP_011523294.1:n.206-45154G>A
XM_017024836.2:c.206-45154G>A	XP_016880325.1:n.206-45154G>A
XM_017024841.1:c.206-45154G>A	XP_016880330.1:n.206-45154G>A
XR_001752558.1:n.418-45154G>A
NM_002737.3:c.206-45154G>A MANE Select	NP_002728.2:n.206-45154G>A