Canonical Allele Identifier: CA407420249
Community Standard Title: NM_002739.5(PRKCG):c.1883C>T (p.Pro628Leu)
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53906435C>T , CM000681.2:g.53906435C>T GRCh38
NC_000019.9:g.54409689C>T , CM000681.1:g.54409689C>T GRCh37
NC_000019.8:g.59101501C>T NCBI36
NG_009114.1:g.29223C>T , LRG_669:g.29223C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002739.5:c.1883C>T MANE Select NP_002730.1:p.Pro628Leu
ENST00000263431.4:c.1883C>T MANE Select ENSP00000263431.3:p.Pro628Leu
NM_001316329.1:c.1883C>T NP_001303258.1:p.Pro628Leu
NM_001316329.2:c.1883C>T NP_001303258.1:p.Pro628Leu
NM_002739.3:c.1883C>T , LRG_669t1:c.1883C>T NP_002730.1:p.Pro628Leu
NM_002739.4:c.1883C>T NP_002730.1:p.Pro628Leu
ENST00000263431.3:c.1883C>T ENSP00000263431.3:p.Pro628Leu
ENST00000682028.1:c.1883C>T ENSP00000507230.1:p.Pro628Leu
ENST00000682676.1:n.1284C>T
ENST00000683513.1:c.1775C>T ENSP00000506809.1:p.Pro592Leu
XM_011527108.1:c.974C>T XP_011525410.1:p.Pro325Leu