Canonical Allele Identifier: CA2271328542

Gene: PRKCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66530870T= , CM000679.2:g.66530870T=	GRCh38
NC_000017.10:g.64526988T= , CM000679.1:g.64526988T=	GRCh37
NC_000017.9:g.61957450T=	NCBI36
NG_012206.1:g.233063T=

Transcript Alleles

HGVS	Amino-acid Change
NM_002737.3:c.288+34587T= MANE Select	NP_002728.2:n.288+34587T=
ENST00000413366.8:c.288+34587T= MANE Select	ENSP00000408695.3:n.288+34587T=
NM_002737.2:c.288+34587T=	NP_002728.1:n.288+34587T=
ENST00000284384.6:c.281-23649T=
ENST00000413366.7:c.288+34587T=	ENSP00000408695.3:n.288+34587T=
ENST00000578063.5:c.288+34587T=	ENSP00000462087.1:n.288+34587T=
XM_011524989.1:c.30+16404T=	XP_011523291.1:n.30+16404T=
XM_011524990.1:c.288+34587T=	XP_011523292.1:n.288+34587T=
XM_011524991.1:c.288+34587T=	XP_011523293.1:n.288+34587T=
XM_011524992.1:c.288+34587T=	XP_011523294.1:n.288+34587T=
XM_017024836.2:c.288+34587T=	XP_016880325.1:n.288+34587T=
XM_017024837.1:c.135+34587T=	XP_016880326.1:n.135+34587T=
XM_017024841.1:c.288+34587T=	XP_016880330.1:n.288+34587T=
XM_024450829.1:c.30+16404T=	XP_024306597.1:n.30+16404T=
XM_024450830.1:c.30+16404T=	XP_024306598.1:n.30+16404T=
XR_001752558.1:n.500+34587T=