Canonical Allele Identifier: CA2392640173

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46366919T= , CM000683.2:g.46366919T=	GRCh38
NC_000021.8:g.47786834T= , CM000683.1:g.47786834T=	GRCh37
NC_000021.7:g.46611262T=	NCBI36
NG_008961.1:g.47799T=
NG_008961.2:g.47798T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1441T=	ENSP00000511987.1:n.*1441T=
ENST00000695525.1:n.3031T=
ENST00000695558.1:c.2945T=	ENSP00000512015.1:p.Ile982=
ENST00000703224.1:c.*2188T=	ENSP00000515242.1:n.*2188T=
ENST00000359568.10:c.2945T= MANE Select	ENSP00000352572.5:p.Ile982=
ENST00000359568.9:c.2945T=	ENSP00000352572.5:p.Ile982=
ENST00000480896.5:n.3214T=
NM_001315529.1:c.2591T=	NP_001302458.1:p.Ile864=
NM_006031.5:c.2945T=	NP_006022.3:p.Ile982=
XM_005261124.3:c.2945T=	XP_005261181.1:p.Ile982=
XM_011529593.1:c.3026T=	XP_011527895.1:p.Ile1009=
XM_011529594.1:c.3026T=	XP_011527896.1:p.Ile1009=
XM_005261124.5:c.2945T=	XP_005261181.1:p.Ile982=
XM_011529594.3:c.3026T=	XP_011527896.1:p.Ile1009=
XM_017028362.2:c.2945T=	XP_016883851.1:p.Ile982=
XM_017028363.1:c.2591T=	XP_016883852.1:p.Ile864=
XM_024452082.1:c.1829T=	XP_024307850.1:p.Ile610=
XM_024452083.1:c.725T=	XP_024307851.1:p.Ile242=
NM_006031.6:c.2945T= MANE Select	NP_006022.3:p.Ile982=
NM_001315529.2:c.2591T=	NP_001302458.1:p.Ile864=