Canonical Allele Identifier: CA410570103

Gene: PCNT

Linked Data

• MyVariant Identifiers: chr21:g.47786923T>A (hg19) ; chr21:g.46367008T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367008T>A , CM000683.2:g.46367008T>A	GRCh38
NC_000021.8:g.47786923T>A , CM000683.1:g.47786923T>A	GRCh37
NC_000021.7:g.46611351T>A	NCBI36
NG_008961.1:g.47888T>A
NG_008961.2:g.47887T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1530T>A	ENSP00000511987.1:n.*1530T>A
ENST00000695525.1:n.3120T>A
ENST00000695558.1:c.3034T>A	ENSP00000512015.1:p.Leu1012Met
ENST00000703224.1:c.*2277T>A	ENSP00000515242.1:n.*2277T>A
ENST00000359568.10:c.3034T>A MANE Select	ENSP00000352572.5:p.Leu1012Met
ENST00000359568.9:c.3034T>A	ENSP00000352572.5:p.Leu1012Met
ENST00000480896.5:n.3303T>A
NM_001315529.1:c.2680T>A	NP_001302458.1:p.Leu894Met
NM_006031.5:c.3034T>A	NP_006022.3:p.Leu1012Met
XM_005261124.3:c.3034T>A	XP_005261181.1:p.Leu1012Met
XM_011529593.1:c.3115T>A	XP_011527895.1:p.Leu1039Met
XM_011529594.1:c.3115T>A	XP_011527896.1:p.Leu1039Met
XM_005261124.5:c.3034T>A	XP_005261181.1:p.Leu1012Met
XM_011529594.3:c.3115T>A	XP_011527896.1:p.Leu1039Met
XM_017028362.2:c.3034T>A	XP_016883851.1:p.Leu1012Met
XM_017028363.1:c.2680T>A	XP_016883852.1:p.Leu894Met
XM_024452082.1:c.1918T>A	XP_024307850.1:p.Leu640Met
XM_024452083.1:c.814T>A	XP_024307851.1:p.Leu272Met
NM_006031.6:c.3034T>A MANE Select	NP_006022.3:p.Leu1012Met
NM_001315529.2:c.2680T>A	NP_001302458.1:p.Leu894Met