Canonical Allele Identifier: CA410557360
Gene: PCNT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46411940C>T , CM000683.2:g.46411940C>T GRCh38
NC_000021.8:g.47831854C>T , CM000683.1:g.47831854C>T GRCh37
NC_000021.7:g.46656282C>T NCBI36
NG_008961.1:g.92819C>T
NG_008961.2:g.92819C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695527.1:n.212C>T
ENST00000695528.1:c.41C>T ENSP00000511990.1:p.Thr14Ile
ENST00000695529.1:n.41C>T
ENST00000695558.1:c.5900C>T ENSP00000512015.1:p.Thr1967Ile
ENST00000703224.1:c.*5110C>T ENSP00000515242.1:n.*5110C>T
ENST00000359568.10:c.5867C>T MANE Select ENSP00000352572.5:p.Thr1956Ile
ENST00000359568.9:c.5867C>T ENSP00000352572.5:p.Thr1956Ile
ENST00000480896.5:n.6136C>T
NM_001315529.1:c.5513C>T NP_001302458.1:p.Thr1838Ile
NM_006031.5:c.5867C>T NP_006022.3:p.Thr1956Ile
XM_005261124.3:c.5900C>T XP_005261181.1:p.Thr1967Ile
XM_011529593.1:c.5978C>T XP_011527895.1:p.Thr1993Ile
XM_011529594.1:c.5948C>T XP_011527896.1:p.Thr1983Ile
XM_005261124.5:c.5900C>T XP_005261181.1:p.Thr1967Ile
XM_011529594.3:c.5948C>T XP_011527896.1:p.Thr1983Ile
XM_017028362.2:c.5867C>T XP_016883851.1:p.Thr1956Ile
XM_017028363.1:c.5546C>T XP_016883852.1:p.Thr1849Ile
XM_024452082.1:c.4784C>T XP_024307850.1:p.Thr1595Ile
XM_024452083.1:c.3680C>T XP_024307851.1:p.Thr1227Ile
NM_006031.6:c.5867C>T MANE Select NP_006022.3:p.Thr1956Ile
NM_001315529.2:c.5513C>T NP_001302458.1:p.Thr1838Ile