Canonical Allele Identifier: CA407418367

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900297-T-A
• MyVariant Identifiers: chr19:g.54403551T>A (hg19) ; chr19:g.53900297T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900297T>A , CM000681.2:g.53900297T>A	GRCh38
NC_000019.9:g.54403551T>A , CM000681.1:g.54403551T>A	GRCh37
NC_000019.8:g.59095363T>A	NCBI36
NG_009114.1:g.23085T>A , LRG_669:g.23085T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1346T>A	ENSP00000507230.1:p.Leu449Gln
ENST00000682268.1:n.1644T>A
ENST00000682676.1:n.747T>A
ENST00000682902.1:n.1648T>A
ENST00000683513.1:c.1346T>A	ENSP00000506809.1:p.Leu449Gln
ENST00000263431.4:c.1346T>A MANE Select	ENSP00000263431.3:p.Leu449Gln
ENST00000263431.3:c.1346T>A	ENSP00000263431.3:p.Leu449Gln
NM_001316329.1:c.1346T>A	NP_001303258.1:p.Leu449Gln
NM_002739.3:c.1346T>A , LRG_669t1:c.1346T>A	NP_002730.1:p.Leu449Gln
NM_002739.4:c.1346T>A	NP_002730.1:p.Leu449Gln
XM_011527108.1:c.437T>A	XP_011525410.1:p.Leu146Gln
NM_002739.5:c.1346T>A MANE Select	NP_002730.1:p.Leu449Gln
NM_001316329.2:c.1346T>A	NP_001303258.1:p.Leu449Gln