Canonical Allele Identifier: CA626924961

Gene: PRKCA

Linked Data

• dbSNP Id: rs1413926459
• gnomAD v2: 17-64788855-C-T
• gnomAD v3: 17-66792737-C-T
• gnomAD v4: 17-66792737-C-T
• MyVariant Identifiers: chr17:g.64788855C>T (hg19) ; chr17:g.66792737C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66792737C>T , CM000679.2:g.66792737C>T	GRCh38
NC_000017.10:g.64788855C>T , CM000679.1:g.64788855C>T	GRCh37
NC_000017.9:g.62219317C>T	NCBI36
NG_012206.1:g.494930C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.1854+3758C>T MANE Select	ENSP00000408695.3:n.1854+3758C>T
ENST00000413366.7:c.1854+3758C>T	ENSP00000408695.3:n.1854+3758C>T
NM_002737.2:c.1854+3758C>T	NP_002728.1:n.1854+3758C>T
XM_011524989.1:c.1597-3711C>T	XP_011523291.1:n.1597-3711C>T
XM_011524990.1:c.1855-3711C>T	XP_011523292.1:n.1855-3711C>T
XM_017024836.2:c.1855-3711C>T	XP_016880325.1:n.1855-3711C>T
XM_017024837.1:c.1701+3758C>T	XP_016880326.1:n.1701+3758C>T
XM_024450829.1:c.1596+3758C>T	XP_024306597.1:n.1596+3758C>T
XM_024450830.1:c.1596+3758C>T	XP_024306598.1:n.1596+3758C>T
NM_002737.3:c.1854+3758C>T MANE Select	NP_002728.2:n.1854+3758C>T