Canonical Allele Identifier: CA633905682

Gene: PRKCG

Linked Data

• dbSNP Id: rs1369225199
• gnomAD v2: 19-54403810-A-C
• gnomAD v3: 19-53900556-A-C
• gnomAD v4: 19-53900556-A-C
• MyVariant Identifiers: chr19:g.54403810A>C (hg19) ; chr19:g.53900556A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900556A>C , CM000681.2:g.53900556A>C	GRCh38
NC_000019.9:g.54403810A>C , CM000681.1:g.54403810A>C	GRCh37
NC_000019.8:g.59095622A>C	NCBI36
NG_009114.1:g.23344A>C , LRG_669:g.23344A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1437-55A>C	ENSP00000507230.1:n.1437-55A>C
ENST00000682268.1:n.1735-55A>C
ENST00000682676.1:n.838-55A>C
ENST00000682902.1:n.1739-55A>C
ENST00000683513.1:c.1437-55A>C	ENSP00000506809.1:n.1437-55A>C
ENST00000263431.4:c.1437-55A>C MANE Select	ENSP00000263431.3:n.1437-55A>C
ENST00000263431.3:c.1437-55A>C	ENSP00000263431.3:n.1437-55A>C
NM_001316329.1:c.1437-55A>C	NP_001303258.1:n.1437-55A>C
NM_002739.3:c.1437-55A>C , LRG_669t1:c.1437-55A>C	NP_002730.1:n.1437-55A>C
NM_002739.4:c.1437-55A>C	NP_002730.1:n.1437-55A>C
XM_011527108.1:c.528-55A>C	XP_011525410.1:n.528-55A>C
NM_002739.5:c.1437-55A>C MANE Select	NP_002730.1:n.1437-55A>C
NM_001316329.2:c.1437-55A>C	NP_001303258.1:n.1437-55A>C