Canonical Allele Identifier: CA209442

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46416737G>A , CM000683.2:g.46416737G>A	GRCh38
NC_000021.8:g.47836651G>A , CM000683.1:g.47836651G>A	GRCh37
NC_000021.7:g.46661079G>A	NCBI36
NG_008961.1:g.97616G>A
NG_008961.2:g.97616G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695527.1:n.1164G>A
ENST00000695528.1:c.993G>A	ENSP00000511990.1:p.Gly331=
ENST00000695529.1:n.993G>A
ENST00000695558.1:c.6852G>A	ENSP00000512015.1:p.Gly2284=
ENST00000703224.1:c.*6062G>A	ENSP00000515242.1:n.*6062G>A
ENST00000359568.10:c.6819G>A MANE Select	ENSP00000352572.5:p.Gly2273=
ENST00000359568.9:c.6819G>A	ENSP00000352572.5:p.Gly2273=
ENST00000480896.5:n.7088G>A
NM_001315529.1:c.6465G>A	NP_001302458.1:p.Gly2155=
NM_006031.5:c.6819G>A	NP_006022.3:p.Gly2273=
XM_005261124.3:c.6852G>A	XP_005261181.1:p.Gly2284=
XM_011529593.1:c.6930G>A	XP_011527895.1:p.Gly2310=
XM_011529594.1:c.6900G>A	XP_011527896.1:p.Gly2300=
XM_005261124.5:c.6852G>A	XP_005261181.1:p.Gly2284=
XM_011529594.3:c.6900G>A	XP_011527896.1:p.Gly2300=
XM_017028362.2:c.6819G>A	XP_016883851.1:p.Gly2273=
XM_017028363.1:c.6498G>A	XP_016883852.1:p.Gly2166=
XM_024452082.1:c.5736G>A	XP_024307850.1:p.Gly1912=
XM_024452083.1:c.4632G>A	XP_024307851.1:p.Gly1544=
NM_006031.6:c.6819G>A MANE Select	NP_006022.3:p.Gly2273=
NM_001315529.2:c.6465G>A	NP_001302458.1:p.Gly2155=