Canonical Allele Identifier: CA985633107

Gene: PRKCA

Linked Data

• dbSNP Id: rs1913780125
• gnomAD v3: 17-66441822-A-G
• gnomAD v4: 17-66441822-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66441822A>G , CM000679.2:g.66441822A>G	GRCh38
NC_000017.10:g.64437940A>G , CM000679.1:g.64437940A>G	GRCh37
NC_000017.9:g.61868402A>G	NCBI36
NG_012206.1:g.144015A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.206-54379A>G MANE Select	ENSP00000408695.3:n.206-54379A>G
ENST00000284384.6:c.198-54379A>G
ENST00000413366.7:c.206-54379A>G	ENSP00000408695.3:n.206-54379A>G
ENST00000578063.5:c.206-54379A>G	ENSP00000462087.1:n.206-54379A>G
NM_002737.2:c.206-54379A>G	NP_002728.1:n.206-54379A>G
XM_011524990.1:c.206-54379A>G	XP_011523292.1:n.206-54379A>G
XM_011524991.1:c.206-54379A>G	XP_011523293.1:n.206-54379A>G
XM_011524992.1:c.206-54379A>G	XP_011523294.1:n.206-54379A>G
XM_017024836.2:c.206-54379A>G	XP_016880325.1:n.206-54379A>G
XM_017024841.1:c.206-54379A>G	XP_016880330.1:n.206-54379A>G
XR_001752558.1:n.418-54379A>G
NM_002737.3:c.206-54379A>G MANE Select	NP_002728.2:n.206-54379A>G