Canonical Allele Identifier: CA410569765

Gene: PCNT

Linked Data

• dbSNP Id: rs1238644889
• gnomAD v4: 21-46366960-G-A
• MyVariant Identifiers: chr21:g.47786875G>A (hg19) ; chr21:g.46366960G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46366960G>A , CM000683.2:g.46366960G>A	GRCh38
NC_000021.8:g.47786875G>A , CM000683.1:g.47786875G>A	GRCh37
NC_000021.7:g.46611303G>A	NCBI36
NG_008961.1:g.47840G>A
NG_008961.2:g.47839G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1482G>A	ENSP00000511987.1:n.*1482G>A
ENST00000695525.1:n.3072G>A
ENST00000695558.1:c.2986G>A	ENSP00000512015.1:p.Asp996Asn
ENST00000703224.1:c.*2229G>A	ENSP00000515242.1:n.*2229G>A
ENST00000359568.10:c.2986G>A MANE Select	ENSP00000352572.5:p.Asp996Asn
ENST00000359568.9:c.2986G>A	ENSP00000352572.5:p.Asp996Asn
ENST00000480896.5:n.3255G>A
NM_001315529.1:c.2632G>A	NP_001302458.1:p.Asp878Asn
NM_006031.5:c.2986G>A	NP_006022.3:p.Asp996Asn
XM_005261124.3:c.2986G>A	XP_005261181.1:p.Asp996Asn
XM_011529593.1:c.3067G>A	XP_011527895.1:p.Asp1023Asn
XM_011529594.1:c.3067G>A	XP_011527896.1:p.Asp1023Asn
XM_005261124.5:c.2986G>A	XP_005261181.1:p.Asp996Asn
XM_011529594.3:c.3067G>A	XP_011527896.1:p.Asp1023Asn
XM_017028362.2:c.2986G>A	XP_016883851.1:p.Asp996Asn
XM_017028363.1:c.2632G>A	XP_016883852.1:p.Asp878Asn
XM_024452082.1:c.1870G>A	XP_024307850.1:p.Asp624Asn
XM_024452083.1:c.766G>A	XP_024307851.1:p.Asp256Asn
NM_006031.6:c.2986G>A MANE Select	NP_006022.3:p.Asp996Asn
NM_001315529.2:c.2632G>A	NP_001302458.1:p.Asp878Asn