Canonical Allele Identifier: CA2271439226

Gene: PRKCA

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66783036T>A , CM000679.2:g.66783036T>A	GRCh38
NC_000017.10:g.64779154T>A , CM000679.1:g.64779154T>A	GRCh37
NC_000017.9:g.62209616T>A	NCBI36
NG_012206.1:g.485229T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413366.8:c.1606-3831T>A MANE Select	ENSP00000408695.3:n.1606-3831T>A
ENST00000413366.7:c.1606-3831T>A	ENSP00000408695.3:n.1606-3831T>A
NM_002737.2:c.1606-3831T>A	NP_002728.1:n.1606-3831T>A
XM_011524989.1:c.1348-3831T>A	XP_011523291.1:n.1348-3831T>A
XM_011524990.1:c.1606-3831T>A	XP_011523292.1:n.1606-3831T>A
XM_017024836.2:c.1606-3831T>A	XP_016880325.1:n.1606-3831T>A
XM_017024837.1:c.1453-3831T>A	XP_016880326.1:n.1453-3831T>A
XM_024450829.1:c.1348-3831T>A	XP_024306597.1:n.1348-3831T>A
XM_024450830.1:c.1348-3831T>A	XP_024306598.1:n.1348-3831T>A
NM_002737.3:c.1606-3831T>A MANE Select	NP_002728.2:n.1606-3831T>A