Canonical Allele Identifier: CA2392640241

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367044G= , CM000683.2:g.46367044G=	GRCh38
NC_000021.8:g.47786959G= , CM000683.1:g.47786959G=	GRCh37
NC_000021.7:g.46611387G=	NCBI36
NG_008961.1:g.47924G=
NG_008961.2:g.47923G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1566G=	ENSP00000511987.1:n.*1566G=
ENST00000695525.1:n.3156G=
ENST00000695558.1:c.3070G=	ENSP00000512015.1:p.Glu1024=
ENST00000703224.1:c.*2313G=	ENSP00000515242.1:n.*2313G=
ENST00000359568.10:c.3070G= MANE Select	ENSP00000352572.5:p.Glu1024=
ENST00000359568.9:c.3070G=	ENSP00000352572.5:p.Glu1024=
ENST00000480896.5:n.3339G=
NM_001315529.1:c.2716G=	NP_001302458.1:p.Glu906=
NM_006031.5:c.3070G=	NP_006022.3:p.Glu1024=
XM_005261124.3:c.3070G=	XP_005261181.1:p.Glu1024=
XM_011529593.1:c.3151G=	XP_011527895.1:p.Glu1051=
XM_011529594.1:c.3151G=	XP_011527896.1:p.Glu1051=
XM_005261124.5:c.3070G=	XP_005261181.1:p.Glu1024=
XM_011529594.3:c.3151G=	XP_011527896.1:p.Glu1051=
XM_017028362.2:c.3070G=	XP_016883851.1:p.Glu1024=
XM_017028363.1:c.2716G=	XP_016883852.1:p.Glu906=
XM_024452082.1:c.1954G=	XP_024307850.1:p.Glu652=
XM_024452083.1:c.850G=	XP_024307851.1:p.Glu284=
NM_006031.6:c.3070G= MANE Select	NP_006022.3:p.Glu1024=
NM_001315529.2:c.2716G=	NP_001302458.1:p.Glu906=