Canonical Allele Identifier: CA2392640260
Gene: PCNT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46367092A= , CM000683.2:g.46367092A= GRCh38
NC_000021.8:g.47787007A= , CM000683.1:g.47787007A= GRCh37
NC_000021.7:g.46611435A= NCBI36
NG_008961.1:g.47972A=
NG_008961.2:g.47971A=

Transcript Alleles

HGVS Amino-acid change
ENST00000466474.6:c.*1614A= ENSP00000511987.1:n.*1614A=
ENST00000695525.1:n.3204A=
ENST00000695558.1:c.3118A= ENSP00000512015.1:p.Thr1040=
ENST00000703224.1:c.*2361A= ENSP00000515242.1:n.*2361A=
ENST00000359568.10:c.3118A= MANE Select ENSP00000352572.5:p.Thr1040=
ENST00000359568.9:c.3118A= ENSP00000352572.5:p.Thr1040=
ENST00000480896.5:n.3387A=
NM_001315529.1:c.2764A= NP_001302458.1:p.Thr922=
NM_006031.5:c.3118A= NP_006022.3:p.Thr1040=
XM_005261124.3:c.3118A= XP_005261181.1:p.Thr1040=
XM_011529593.1:c.3199A= XP_011527895.1:p.Thr1067=
XM_011529594.1:c.3199A= XP_011527896.1:p.Thr1067=
XM_005261124.5:c.3118A= XP_005261181.1:p.Thr1040=
XM_011529594.3:c.3199A= XP_011527896.1:p.Thr1067=
XM_017028362.2:c.3118A= XP_016883851.1:p.Thr1040=
XM_017028363.1:c.2764A= XP_016883852.1:p.Thr922=
XM_024452082.1:c.2002A= XP_024307850.1:p.Thr668=
XM_024452083.1:c.898A= XP_024307851.1:p.Thr300=
NM_006031.6:c.3118A= MANE Select NP_006022.3:p.Thr1040=
NM_001315529.2:c.2764A= NP_001302458.1:p.Thr922=