Canonical Allele Identifier: CA205361

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46391300G>A , CM000683.2:g.46391300G>A	GRCh38
NC_000021.8:g.47811215G>A , CM000683.1:g.47811215G>A	GRCh37
NC_000021.7:g.46635643G>A	NCBI36
NG_008961.1:g.72180G>A
NG_008961.2:g.72179G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695558.1:c.4140G>A	ENSP00000512015.1:p.Ala1380=
ENST00000703224.1:c.*3383G>A	ENSP00000515242.1:n.*3383G>A
ENST00000359568.10:c.4140G>A MANE Select	ENSP00000352572.5:p.Ala1380=
ENST00000359568.9:c.4140G>A	ENSP00000352572.5:p.Ala1380=
ENST00000480896.5:n.4409G>A
NM_001315529.1:c.3786G>A	NP_001302458.1:p.Ala1262=
NM_006031.5:c.4140G>A	NP_006022.3:p.Ala1380=
XM_005261124.3:c.4140G>A	XP_005261181.1:p.Ala1380=
XM_011529593.1:c.4221G>A	XP_011527895.1:p.Ala1407=
XM_011529594.1:c.4221G>A	XP_011527896.1:p.Ala1407=
XM_005261124.5:c.4140G>A	XP_005261181.1:p.Ala1380=
XM_011529594.3:c.4221G>A	XP_011527896.1:p.Ala1407=
XM_017028362.2:c.4140G>A	XP_016883851.1:p.Ala1380=
XM_017028363.1:c.3786G>A	XP_016883852.1:p.Ala1262=
XM_024452082.1:c.3024G>A	XP_024307850.1:p.Ala1008=
XM_024452083.1:c.1920G>A	XP_024307851.1:p.Ala640=
NM_006031.6:c.4140G>A MANE Select	NP_006022.3:p.Ala1380=
NM_001315529.2:c.3786G>A	NP_001302458.1:p.Ala1262=