Canonical Allele Identifier: CA627134063

Gene: PRKCA

Linked Data

• dbSNP Id: rs1359694260
• gnomAD v2: 17-64437797-GCTGCTGTGCGGTTTTTTCAAC-G
• MyVariant Identifiers: chr17:g.64437798_64437818del (hg19) ; chr17:g.66441680_66441700del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66441683_66441703del , CM000679.2:g.66441683_66441703del	GRCh38
NC_000017.10:g.64437801_64437821del , CM000679.1:g.64437801_64437821del	GRCh37
NC_000017.9:g.61868263_61868283del	NCBI36
NG_012206.1:g.143876_143896del

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.206-54518_206-54498del MANE Select	ENSP00000408695.3:n.206-54518_206-54498del
ENST00000284384.6:c.198-54518_198-54498del
ENST00000413366.7:c.206-54518_206-54498del	ENSP00000408695.3:n.206-54518_206-54498del
ENST00000578063.5:c.206-54518_206-54498del	ENSP00000462087.1:n.206-54518_206-54498del
NM_002737.2:c.206-54518_206-54498del	NP_002728.1:n.206-54518_206-54498del
XM_011524990.1:c.206-54518_206-54498del	XP_011523292.1:n.206-54518_206-54498del
XM_011524991.1:c.206-54518_206-54498del	XP_011523293.1:n.206-54518_206-54498del
XM_011524992.1:c.206-54518_206-54498del	XP_011523294.1:n.206-54518_206-54498del
XM_017024836.2:c.206-54518_206-54498del	XP_016880325.1:n.206-54518_206-54498del
XM_017024841.1:c.206-54518_206-54498del	XP_016880330.1:n.206-54518_206-54498del
XR_001752558.1:n.418-54518_418-54498del
NM_002737.3:c.206-54518_206-54498del MANE Select	NP_002728.2:n.206-54518_206-54498del