Canonical Allele Identifier: CA310078766

Gene: PRKCG

Linked Data

• dbSNP Id: rs941200894
• gnomAD v3: 19-53882231-CGCCGCCGCCCGTGCCTCCGGCT-C
• gnomAD v4: 19-53882231-CGCCGCCGCCCGTGCCTCCGGCT-C
• MyVariant Identifiers: chr19:g.54385486_54385507del (hg19) ; chr19:g.53882232_53882253del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882236_53882257del , CM000681.2:g.53882236_53882257del	GRCh38
NC_000019.9:g.54385490_54385511del , CM000681.1:g.54385490_54385511del	GRCh37
NC_000019.8:g.59077302_59077323del	NCBI36
NG_009114.1:g.5024_5045del , LRG_669:g.5024_5045del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-259_-238del	ENSP00000507230.1:n.-259_-238del
ENST00000682268.1:n.40_61del
ENST00000682902.1:n.44_65del
ENST00000683513.1:c.-259_-238del	ENSP00000506809.1:n.-259_-238del
ENST00000263431.4:c.-259_-238del MANE Select	ENSP00000263431.3:n.-259_-238del
ENST00000263431.3:c.-259_-238del	ENSP00000263431.3:n.-259_-238del
ENST00000419486.1:c.-446_-425del	ENSP00000387919.2:n.-446_-425del
ENST00000474397.5:c.-322-321_-322-300del	ENSP00000471271.1:n.-322-321_-322-300del
ENST00000479081.5:c.-322-321_-322-300del	ENSP00000471544.1:n.-322-321_-322-300del
NM_001316329.1:c.-259_-238del	NP_001303258.1:n.-259_-238del
NM_002739.3:c.-259_-238del , LRG_669t1:c.-259_-238del	NP_002730.1:n.-259_-238del
NM_002739.4:c.-259_-238del	NP_002730.1:n.-259_-238del
NM_002739.5:c.-259_-238del MANE Select	NP_002730.1:n.-259_-238del
NM_001316329.2:c.-259_-238del	NP_001303258.1:n.-259_-238del