Canonical Allele Identifier: CA2392640259

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367088G= , CM000683.2:g.46367088G=	GRCh38
NC_000021.8:g.47787003G= , CM000683.1:g.47787003G=	GRCh37
NC_000021.7:g.46611431G=	NCBI36
NG_008961.1:g.47968G=
NG_008961.2:g.47967G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1610G=	ENSP00000511987.1:n.*1610G=
ENST00000695525.1:n.3200G=
ENST00000695558.1:c.3114G=	ENSP00000512015.1:p.Val1038=
ENST00000703224.1:c.*2357G=	ENSP00000515242.1:n.*2357G=
ENST00000359568.10:c.3114G= MANE Select	ENSP00000352572.5:p.Val1038=
ENST00000359568.9:c.3114G=	ENSP00000352572.5:p.Val1038=
ENST00000480896.5:n.3383G=
NM_001315529.1:c.2760G=	NP_001302458.1:p.Val920=
NM_006031.5:c.3114G=	NP_006022.3:p.Val1038=
XM_005261124.3:c.3114G=	XP_005261181.1:p.Val1038=
XM_011529593.1:c.3195G=	XP_011527895.1:p.Val1065=
XM_011529594.1:c.3195G=	XP_011527896.1:p.Val1065=
XM_005261124.5:c.3114G=	XP_005261181.1:p.Val1038=
XM_011529594.3:c.3195G=	XP_011527896.1:p.Val1065=
XM_017028362.2:c.3114G=	XP_016883851.1:p.Val1038=
XM_017028363.1:c.2760G=	XP_016883852.1:p.Val920=
XM_024452082.1:c.1998G=	XP_024307850.1:p.Val666=
XM_024452083.1:c.894G=	XP_024307851.1:p.Val298=
NM_006031.6:c.3114G= MANE Select	NP_006022.3:p.Val1038=
NM_001315529.2:c.2760G=	NP_001302458.1:p.Val920=