Canonical Allele Identifier: CA410570523

Gene: PCNT

Linked Data

• gnomAD v4: 21-46367091-C-A
• MyVariant Identifiers: chr21:g.47787006C>A (hg19) ; chr21:g.46367091C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367091C>A , CM000683.2:g.46367091C>A	GRCh38
NC_000021.8:g.47787006C>A , CM000683.1:g.47787006C>A	GRCh37
NC_000021.7:g.46611434C>A	NCBI36
NG_008961.1:g.47971C>A
NG_008961.2:g.47970C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1613C>A	ENSP00000511987.1:n.*1613C>A
ENST00000695525.1:n.3203C>A
ENST00000695558.1:c.3117C>A	ENSP00000512015.1:p.Ser1039Arg
ENST00000703224.1:c.*2360C>A	ENSP00000515242.1:n.*2360C>A
ENST00000359568.10:c.3117C>A MANE Select	ENSP00000352572.5:p.Ser1039Arg
ENST00000359568.9:c.3117C>A	ENSP00000352572.5:p.Ser1039Arg
ENST00000480896.5:n.3386C>A
NM_001315529.1:c.2763C>A	NP_001302458.1:p.Ser921Arg
NM_006031.5:c.3117C>A	NP_006022.3:p.Ser1039Arg
XM_005261124.3:c.3117C>A	XP_005261181.1:p.Ser1039Arg
XM_011529593.1:c.3198C>A	XP_011527895.1:p.Ser1066Arg
XM_011529594.1:c.3198C>A	XP_011527896.1:p.Ser1066Arg
XM_005261124.5:c.3117C>A	XP_005261181.1:p.Ser1039Arg
XM_011529594.3:c.3198C>A	XP_011527896.1:p.Ser1066Arg
XM_017028362.2:c.3117C>A	XP_016883851.1:p.Ser1039Arg
XM_017028363.1:c.2763C>A	XP_016883852.1:p.Ser921Arg
XM_024452082.1:c.2001C>A	XP_024307850.1:p.Ser667Arg
XM_024452083.1:c.897C>A	XP_024307851.1:p.Ser299Arg
NM_006031.6:c.3117C>A MANE Select	NP_006022.3:p.Ser1039Arg
NM_001315529.2:c.2763C>A	NP_001302458.1:p.Ser921Arg