Canonical Allele Identifier: CA236167
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 127247
dbSNP Id: rs587779355

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46326518G>T , CM000683.2:g.46326518G>T GRCh38
NC_000021.8:g.47746432G>T , CM000683.1:g.47746432G>T GRCh37
NC_000021.7:g.46570860G>T NCBI36
NG_008961.1:g.7397G>T
NG_008961.2:g.7397G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000466474.6:c.196G>T ENSP00000511987.1:p.Gly66Ter
ENST00000695525.1:n.282G>T
ENST00000695526.1:c.196G>T ENSP00000511988.1:p.Gly66Ter
ENST00000695558.1:c.196G>T ENSP00000512015.1:p.Gly66Ter
ENST00000703224.1:c.196G>T ENSP00000515242.1:p.Gly66Ter
ENST00000703225.1:n.1631G>T
ENST00000359568.10:c.196G>T MANE Select ENSP00000352572.5:p.Gly66Ter
ENST00000359568.9:c.196G>T ENSP00000352572.5:p.Gly66Ter
ENST00000480896.5:n.465G>T
ENST00000490468.5:n.284G>T
NM_001315529.1:c.-159G>T NP_001302458.1:n.-159G>T
NM_006031.5:c.196G>T NP_006022.3:p.Gly66Ter
XM_005261124.3:c.196G>T XP_005261181.1:p.Gly66Ter
XM_011529593.1:c.196G>T XP_011527895.1:p.Gly66Ter
XM_011529594.1:c.196G>T XP_011527896.1:p.Gly66Ter
XM_005261124.5:c.196G>T XP_005261181.1:p.Gly66Ter
XM_011529594.3:c.196G>T XP_011527896.1:p.Gly66Ter
XM_017028362.2:c.196G>T XP_016883851.1:p.Gly66Ter
XM_017028363.1:c.-159G>T XP_016883852.1:n.-159G>T
XM_024452083.1:c.-1913G>T XP_024307851.1:n.-1913G>T
NM_006031.6:c.196G>T MANE Select NP_006022.3:p.Gly66Ter
NM_001315529.2:c.-159G>T NP_001302458.1:n.-159G>T