Canonical Allele Identifier: CA2392632185
Gene: PCNT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46353125C= , CM000683.2:g.46353125C= GRCh38
NC_000021.8:g.47773039C= , CM000683.1:g.47773039C= GRCh37
NC_000021.7:g.46597467C= NCBI36
NG_008961.1:g.34004C=
NG_008961.2:g.34004C=

Transcript Alleles

HGVS Amino-acid change
ENST00000466474.6:c.1366C= ENSP00000511987.1:p.Arg456=
ENST00000695525.1:n.1564C=
ENST00000695526.1:c.1403C= ENSP00000511988.1:p.Ala468=
ENST00000695558.1:c.1478C= ENSP00000512015.1:p.Ala493=
ENST00000703224.1:c.*721C= ENSP00000515242.1:n.*721C=
ENST00000359568.10:c.1478C= MANE Select ENSP00000352572.5:p.Ala493=
ENST00000359568.9:c.1478C= ENSP00000352572.5:p.Ala493=
ENST00000466474.5:n.717C=
ENST00000480896.5:n.1747C=
ENST00000483844.1:n.533C=
NM_001315529.1:c.1124C= NP_001302458.1:p.Ala375=
NM_006031.5:c.1478C= NP_006022.3:p.Ala493=
XM_005261124.3:c.1478C= XP_005261181.1:p.Ala493=
XM_011529593.1:c.1559C= XP_011527895.1:p.Ala520=
XM_011529594.1:c.1559C= XP_011527896.1:p.Ala520=
XM_005261124.5:c.1478C= XP_005261181.1:p.Ala493=
XM_011529594.3:c.1559C= XP_011527896.1:p.Ala520=
XM_017028362.2:c.1478C= XP_016883851.1:p.Ala493=
XM_017028363.1:c.1124C= XP_016883852.1:p.Ala375=
XM_024452082.1:c.362C= XP_024307850.1:p.Ala121=
XM_024452083.1:c.-743C= XP_024307851.1:n.-743C=
NM_006031.6:c.1478C= MANE Select NP_006022.3:p.Ala493=
NM_001315529.2:c.1124C= NP_001302458.1:p.Ala375=