Canonical Allele Identifier: CA2271443498

Gene: PRKCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66792745G= , CM000679.2:g.66792745G=	GRCh38
NC_000017.10:g.64788863G= , CM000679.1:g.64788863G=	GRCh37
NC_000017.9:g.62219325G=	NCBI36
NG_012206.1:g.494938G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.1854+3766G= MANE Select	ENSP00000408695.3:n.1854+3766G=
ENST00000413366.7:c.1854+3766G=	ENSP00000408695.3:n.1854+3766G=
NM_002737.2:c.1854+3766G=	NP_002728.1:n.1854+3766G=
XM_011524989.1:c.1597-3703G=	XP_011523291.1:n.1597-3703G=
XM_011524990.1:c.1855-3703G=	XP_011523292.1:n.1855-3703G=
XM_017024836.2:c.1855-3703G=	XP_016880325.1:n.1855-3703G=
XM_017024837.1:c.1701+3766G=	XP_016880326.1:n.1701+3766G=
XM_024450829.1:c.1596+3766G=	XP_024306597.1:n.1596+3766G=
XM_024450830.1:c.1596+3766G=	XP_024306598.1:n.1596+3766G=
NM_002737.3:c.1854+3766G= MANE Select	NP_002728.2:n.1854+3766G=