Canonical Allele Identifier: CA774243979

Gene: PRKCA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66441893C>T , CM000679.2:g.66441893C>T	GRCh38
NC_000017.10:g.64438011C>T , CM000679.1:g.64438011C>T	GRCh37
NC_000017.9:g.61868473C>T	NCBI36
NG_012206.1:g.144086C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413366.8:c.206-54308C>T MANE Select	ENSP00000408695.3:n.206-54308C>T
ENST00000284384.6:c.198-54308C>T
ENST00000413366.7:c.206-54308C>T	ENSP00000408695.3:n.206-54308C>T
ENST00000578063.5:c.206-54308C>T	ENSP00000462087.1:n.206-54308C>T
NM_002737.2:c.206-54308C>T	NP_002728.1:n.206-54308C>T
XM_011524990.1:c.206-54308C>T	XP_011523292.1:n.206-54308C>T
XM_011524991.1:c.206-54308C>T	XP_011523293.1:n.206-54308C>T
XM_011524992.1:c.206-54308C>T	XP_011523294.1:n.206-54308C>T
XM_017024836.2:c.206-54308C>T	XP_016880325.1:n.206-54308C>T
XM_017024841.1:c.206-54308C>T	XP_016880330.1:n.206-54308C>T
XR_001752558.1:n.418-54308C>T
NM_002737.3:c.206-54308C>T MANE Select	NP_002728.2:n.206-54308C>T