Canonical Allele Identifier: CA2392628498

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46346146G= , CM000683.2:g.46346146G=	GRCh38
NC_000021.8:g.47766060G= , CM000683.1:g.47766060G=	GRCh37
NC_000021.7:g.46590488G=	NCBI36
NG_008961.1:g.27025G=
NG_008961.2:g.27025G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006031.6:c.658G= MANE Select	NP_006022.3:p.Glu220=
ENST00000359568.10:c.658G= MANE Select	ENSP00000352572.5:p.Glu220=
NM_001315529.1:c.304G=	NP_001302458.1:p.Glu102=
NM_001315529.2:c.304G=	NP_001302458.1:p.Glu102=
NM_006031.5:c.658G=	NP_006022.3:p.Glu220=
ENST00000359568.9:c.658G=	ENSP00000352572.5:p.Glu220=
ENST00000466474.5:n.9G=
ENST00000466474.6:c.658G=	ENSP00000511987.1:p.Glu220=
ENST00000480896.5:n.927G=
ENST00000490468.5:n.746G=
ENST00000695525.1:n.744G=
ENST00000695526.1:c.583G=	ENSP00000511988.1:p.Glu195=
ENST00000695558.1:c.658G=	ENSP00000512015.1:p.Glu220=
ENST00000703224.1:c.831G=	ENSP00000515242.1:p.Val277=
ENST00000703225.1:n.2093G=
XM_005261124.3:c.658G=	XP_005261181.1:p.Glu220=
XM_005261124.5:c.658G=	XP_005261181.1:p.Glu220=
XM_011529593.1:c.739G=	XP_011527895.1:p.Glu247=
XM_011529594.1:c.739G=	XP_011527896.1:p.Glu247=
XM_011529594.3:c.739G=	XP_011527896.1:p.Glu247=
XM_017028362.2:c.658G=	XP_016883851.1:p.Glu220=
XM_017028363.1:c.304G=	XP_016883852.1:p.Glu102=
XM_024452083.1:c.-1451G=	XP_024307851.1:n.-1451G=