Canonical Allele Identifier: CA407418632

Gene: PRKCG

Linked Data

• MyVariant Identifiers: chr19:g.54403881A>C (hg19) ; chr19:g.53900627A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900627A>C , CM000681.2:g.53900627A>C	GRCh38
NC_000019.9:g.54403881A>C , CM000681.1:g.54403881A>C	GRCh37
NC_000019.8:g.59095693A>C	NCBI36
NG_009114.1:g.23415A>C , LRG_669:g.23415A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1453A>C	ENSP00000507230.1:p.Asn485His
ENST00000682268.1:n.1751A>C
ENST00000682676.1:n.854A>C
ENST00000682902.1:n.1755A>C
ENST00000683513.1:c.1453A>C	ENSP00000506809.1:p.Asn485His
ENST00000263431.4:c.1453A>C MANE Select	ENSP00000263431.3:p.Asn485His
ENST00000263431.3:c.1453A>C	ENSP00000263431.3:p.Asn485His
NM_001316329.1:c.1453A>C	NP_001303258.1:p.Asn485His
NM_002739.3:c.1453A>C , LRG_669t1:c.1453A>C	NP_002730.1:p.Asn485His
NM_002739.4:c.1453A>C	NP_002730.1:p.Asn485His
XM_011527108.1:c.544A>C	XP_011525410.1:p.Asn182His
NM_002739.5:c.1453A>C MANE Select	NP_002730.1:p.Asn485His
NM_001316329.2:c.1453A>C	NP_001303258.1:p.Asn485His