Canonical Allele Identifier: CA2271420473

Gene: PRKCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66740112C= , CM000679.2:g.66740112C=	GRCh38
NC_000017.10:g.64736230C= , CM000679.1:g.64736230C=	GRCh37
NC_000017.9:g.62166692C=	NCBI36
NG_012206.1:g.442305C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002737.3:c.1322+1257C= MANE Select	NP_002728.2:n.1322+1257C=
ENST00000413366.8:c.1322+1257C= MANE Select	ENSP00000408695.3:n.1322+1257C=
NM_002737.2:c.1322+1257C=	NP_002728.1:n.1322+1257C=
ENST00000284384.6:c.1375+1257C=
ENST00000413366.7:c.1322+1257C=	ENSP00000408695.3:n.1322+1257C=
XM_011524989.1:c.1064+1257C=	XP_011523291.1:n.1064+1257C=
XM_011524990.1:c.1322+1257C=	XP_011523292.1:n.1322+1257C=
XM_017024836.2:c.1322+1257C=	XP_016880325.1:n.1322+1257C=
XM_017024837.1:c.1169+1257C=	XP_016880326.1:n.1169+1257C=
XM_024450829.1:c.1064+1257C=	XP_024306597.1:n.1064+1257C=
XM_024450830.1:c.1064+1257C=	XP_024306598.1:n.1064+1257C=