Canonical Allele Identifier: CA2271443504

Gene: PRKCA

Linked Data

• dbSNP Id: rs1975572097

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66792754G>C , CM000679.2:g.66792754G>C	GRCh38
NC_000017.10:g.64788872G>C , CM000679.1:g.64788872G>C	GRCh37
NC_000017.9:g.62219334G>C	NCBI36
NG_012206.1:g.494947G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.1854+3775G>C MANE Select	ENSP00000408695.3:n.1854+3775G>C
ENST00000413366.7:c.1854+3775G>C	ENSP00000408695.3:n.1854+3775G>C
NM_002737.2:c.1854+3775G>C	NP_002728.1:n.1854+3775G>C
XM_011524989.1:c.1597-3694G>C	XP_011523291.1:n.1597-3694G>C
XM_011524990.1:c.1855-3694G>C	XP_011523292.1:n.1855-3694G>C
XM_017024836.2:c.1855-3694G>C	XP_016880325.1:n.1855-3694G>C
XM_017024837.1:c.1701+3775G>C	XP_016880326.1:n.1701+3775G>C
XM_024450829.1:c.1596+3775G>C	XP_024306597.1:n.1596+3775G>C
XM_024450830.1:c.1596+3775G>C	XP_024306598.1:n.1596+3775G>C
NM_002737.3:c.1854+3775G>C MANE Select	NP_002728.2:n.1854+3775G>C