Canonical Allele Identifier: CA2392640210
Gene: PCNT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46366991C= , CM000683.2:g.46366991C= GRCh38
NC_000021.8:g.47786906C= , CM000683.1:g.47786906C= GRCh37
NC_000021.7:g.46611334C= NCBI36
NG_008961.1:g.47871C=
NG_008961.2:g.47870C=

Transcript Alleles

HGVS Amino-acid change
ENST00000466474.6:c.*1513C= ENSP00000511987.1:n.*1513C=
ENST00000695525.1:n.3103C=
ENST00000695558.1:c.3017C= ENSP00000512015.1:p.Ser1006=
ENST00000703224.1:c.*2260C= ENSP00000515242.1:n.*2260C=
ENST00000359568.10:c.3017C= MANE Select ENSP00000352572.5:p.Ser1006=
ENST00000359568.9:c.3017C= ENSP00000352572.5:p.Ser1006=
ENST00000480896.5:n.3286C=
NM_001315529.1:c.2663C= NP_001302458.1:p.Ser888=
NM_006031.5:c.3017C= NP_006022.3:p.Ser1006=
XM_005261124.3:c.3017C= XP_005261181.1:p.Ser1006=
XM_011529593.1:c.3098C= XP_011527895.1:p.Ser1033=
XM_011529594.1:c.3098C= XP_011527896.1:p.Ser1033=
XM_005261124.5:c.3017C= XP_005261181.1:p.Ser1006=
XM_011529594.3:c.3098C= XP_011527896.1:p.Ser1033=
XM_017028362.2:c.3017C= XP_016883851.1:p.Ser1006=
XM_017028363.1:c.2663C= XP_016883852.1:p.Ser888=
XM_024452082.1:c.1901C= XP_024307850.1:p.Ser634=
XM_024452083.1:c.797C= XP_024307851.1:p.Ser266=
NM_006031.6:c.3017C= MANE Select NP_006022.3:p.Ser1006=
NM_001315529.2:c.2663C= NP_001302458.1:p.Ser888=