Canonical Allele Identifier: CA2392638079
Community Standard Title: NM_006031.6(PCNT):c.2374C= (p.Arg792=)
Gene: PCNT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46363699C= , CM000683.2:g.46363699C= GRCh38
NC_000021.8:g.47783614C= , CM000683.1:g.47783614C= GRCh37
NC_000021.7:g.46608042C= NCBI36
NG_008961.1:g.44579C=
NG_008961.2:g.44578C=

Transcript Alleles

HGVS Amino-acid Change
NM_006031.6:c.2374C= MANE Select NP_006022.3:p.Arg792=
ENST00000359568.10:c.2374C= MANE Select ENSP00000352572.5:p.Arg792=
NM_001315529.1:c.2020C= NP_001302458.1:p.Arg674=
NM_001315529.2:c.2020C= NP_001302458.1:p.Arg674=
NM_006031.5:c.2374C= NP_006022.3:p.Arg792=
ENST00000359568.9:c.2374C= ENSP00000352572.5:p.Arg792=
ENST00000466474.6:c.*870C= ENSP00000511987.1:n.*870C=
ENST00000480896.5:n.2643C=
ENST00000695525.1:n.2460C=
ENST00000695558.1:c.2374C= ENSP00000512015.1:p.Arg792=
ENST00000703224.1:c.*1617C= ENSP00000515242.1:n.*1617C=
XM_005261124.3:c.2374C= XP_005261181.1:p.Arg792=
XM_005261124.5:c.2374C= XP_005261181.1:p.Arg792=
XM_011529593.1:c.2455C= XP_011527895.1:p.Arg819=
XM_011529594.1:c.2455C= XP_011527896.1:p.Arg819=
XM_011529594.3:c.2455C= XP_011527896.1:p.Arg819=
XM_017028362.2:c.2374C= XP_016883851.1:p.Arg792=
XM_017028363.1:c.2020C= XP_016883852.1:p.Arg674=
XM_024452082.1:c.1258C= XP_024307850.1:p.Arg420=
XM_024452083.1:c.154C= XP_024307851.1:p.Arg52=