Canonical Allele Identifier: CA2392678660

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46435904C= , CM000683.2:g.46435904C=	GRCh38
NC_000021.8:g.47855817C= , CM000683.1:g.47855817C=	GRCh37
NC_000021.7:g.46680245C=	NCBI36
NG_008961.1:g.116782C=
NG_008961.2:g.116783C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006031.6:c.8752C= MANE Select	NP_006022.3:p.Arg2918=
ENST00000359568.10:c.8752C= MANE Select	ENSP00000352572.5:p.Arg2918=
NM_001315529.1:c.8161C=	NP_001302458.1:p.Arg2721=
NM_001315529.2:c.8161C=	NP_001302458.1:p.Arg2721=
NM_006031.5:c.8752C=	NP_006022.3:p.Arg2918=
ENST00000359568.9:c.8752C=	ENSP00000352572.5:p.Arg2918=
ENST00000418394.2:c.1334C=
ENST00000480896.5:n.8784C=
ENST00000695527.1:n.3097C=
ENST00000695528.1:c.2785C=	ENSP00000511990.1:p.Arg929=
ENST00000695529.1:n.2548C=
ENST00000695530.1:c.1334C=
ENST00000695531.1:n.2354C=
ENST00000695532.1:n.2354C=
ENST00000695533.1:n.1422C=
ENST00000695534.1:n.1146C=
ENST00000695535.1:n.227C=
ENST00000695558.1:c.8785C=	ENSP00000512015.1:p.Arg2929=
ENST00000703224.1:c.*7995C=	ENSP00000515242.1:n.*7995C=
ENST00000703226.1:n.1422C=
XM_005261124.3:c.8785C=	XP_005261181.1:p.Arg2929=
XM_005261124.5:c.8785C=	XP_005261181.1:p.Arg2929=
XM_011529593.1:c.8863C=	XP_011527895.1:p.Arg2955=
XM_011529594.1:c.8833C=	XP_011527896.1:p.Arg2945=
XM_011529594.3:c.8833C=	XP_011527896.1:p.Arg2945=
XM_017028362.2:c.8515C=	XP_016883851.1:p.Arg2839=
XM_017028363.1:c.8431C=	XP_016883852.1:p.Arg2811=
XM_024452082.1:c.7669C=	XP_024307850.1:p.Arg2557=
XM_024452083.1:c.6565C=	XP_024307851.1:p.Arg2189=