Canonical Allele Identifier: CA293510257

Gene: PRKCA

Linked Data

• dbSNP Id: rs371236344
• gnomAD v2: 17-64437857-C-CT
• gnomAD v3: 17-66441739-C-CT
• gnomAD v4: 17-66441739-C-CT
• MyVariant Identifiers: chr17:g.64437858_64437859insT (hg19) ; chr17:g.64437857_64437858insT (hg19) ; chr17:g.66441740_66441741insT (hg38) ; chr17:g.66441739_66441740insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66441748dup , CM000679.2:g.66441748dup	GRCh38
NC_000017.10:g.64437866dup , CM000679.1:g.64437866dup	GRCh37
NC_000017.9:g.61868328dup	NCBI36
NG_012206.1:g.143941dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.206-54453dup MANE Select	ENSP00000408695.3:n.206-54453dup
ENST00000284384.6:c.198-54453dup
ENST00000413366.7:c.206-54453dup	ENSP00000408695.3:n.206-54453dup
ENST00000578063.5:c.206-54453dup	ENSP00000462087.1:n.206-54453dup
NM_002737.2:c.206-54453dup	NP_002728.1:n.206-54453dup
XM_011524990.1:c.206-54453dup	XP_011523292.1:n.206-54453dup
XM_011524991.1:c.206-54453dup	XP_011523293.1:n.206-54453dup
XM_011524992.1:c.206-54453dup	XP_011523294.1:n.206-54453dup
XM_017024836.2:c.206-54453dup	XP_016880325.1:n.206-54453dup
XM_017024841.1:c.206-54453dup	XP_016880330.1:n.206-54453dup
XR_001752558.1:n.418-54453dup
NM_002737.3:c.206-54453dup MANE Select	NP_002728.2:n.206-54453dup