Canonical Allele Identifier: CA774300239

Gene: PRKCA

Linked Data

• dbSNP Id: rs1180467349
• gnomAD v3: 17-66792768-T-C
• gnomAD v4: 17-66792768-T-C
• MyVariant Identifiers: chr17:g.64788886T>C (hg19) ; chr17:g.66792768T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66792768T>C , CM000679.2:g.66792768T>C	GRCh38
NC_000017.10:g.64788886T>C , CM000679.1:g.64788886T>C	GRCh37
NC_000017.9:g.62219348T>C	NCBI36
NG_012206.1:g.494961T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.1854+3789T>C MANE Select	ENSP00000408695.3:n.1854+3789T>C
ENST00000413366.7:c.1854+3789T>C	ENSP00000408695.3:n.1854+3789T>C
NM_002737.2:c.1854+3789T>C	NP_002728.1:n.1854+3789T>C
XM_011524989.1:c.1597-3680T>C	XP_011523291.1:n.1597-3680T>C
XM_011524990.1:c.1855-3680T>C	XP_011523292.1:n.1855-3680T>C
XM_017024836.2:c.1855-3680T>C	XP_016880325.1:n.1855-3680T>C
XM_017024837.1:c.1701+3789T>C	XP_016880326.1:n.1701+3789T>C
XM_024450829.1:c.1596+3789T>C	XP_024306597.1:n.1596+3789T>C
XM_024450830.1:c.1596+3789T>C	XP_024306598.1:n.1596+3789T>C
NM_002737.3:c.1854+3789T>C MANE Select	NP_002728.2:n.1854+3789T>C