Canonical Allele Identifier: CA293171637

Gene: PRKCA

Linked Data

• dbSNP Id: rs971070927
• gnomAD v2: 17-64788863-G-A
• gnomAD v3: 17-66792745-G-A
• gnomAD v4: 17-66792745-G-A
• MyVariant Identifiers: chr17:g.64788863G>A (hg19) ; chr17:g.66792745G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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