Canonical Allele Identifier: CA2271443464

Gene: PRKCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66792641A= , CM000679.2:g.66792641A=	GRCh38
NC_000017.10:g.64788759A= , CM000679.1:g.64788759A=	GRCh37
NC_000017.9:g.62219221A=	NCBI36
NG_012206.1:g.494834A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413366.8:c.1854+3662A= MANE Select	ENSP00000408695.3:n.1854+3662A=
ENST00000413366.7:c.1854+3662A=	ENSP00000408695.3:n.1854+3662A=
NM_002737.2:c.1854+3662A=	NP_002728.1:n.1854+3662A=
XM_011524989.1:c.1596+3662A=	XP_011523291.1:n.1596+3662A=
XM_011524990.1:c.1854+3662A=	XP_011523292.1:n.1854+3662A=
XM_017024836.2:c.1854+3662A=	XP_016880325.1:n.1854+3662A=
XM_017024837.1:c.1701+3662A=	XP_016880326.1:n.1701+3662A=
XM_024450829.1:c.1596+3662A=	XP_024306597.1:n.1596+3662A=
XM_024450830.1:c.1596+3662A=	XP_024306598.1:n.1596+3662A=
NM_002737.3:c.1854+3662A= MANE Select	NP_002728.2:n.1854+3662A=