Canonical Allele Identifier: CA10080275

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46416103C>T , CM000683.2:g.46416103C>T	GRCh38
NC_000021.8:g.47836017C>T , CM000683.1:g.47836017C>T	GRCh37
NC_000021.7:g.46660445C>T	NCBI36
NG_008961.1:g.96982C>T
NG_008961.2:g.96982C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695527.1:n.530C>T
ENST00000695528.1:c.359C>T	ENSP00000511990.1:p.Pro120Leu
ENST00000695529.1:n.359C>T
ENST00000695558.1:c.6218C>T	ENSP00000512015.1:p.Pro2073Leu
ENST00000703224.1:c.*5428C>T	ENSP00000515242.1:n.*5428C>T
ENST00000359568.10:c.6185C>T MANE Select	ENSP00000352572.5:p.Pro2062Leu
ENST00000359568.9:c.6185C>T	ENSP00000352572.5:p.Pro2062Leu
ENST00000480896.5:n.6454C>T
NM_001315529.1:c.5831C>T	NP_001302458.1:p.Pro1944Leu
NM_006031.5:c.6185C>T	NP_006022.3:p.Pro2062Leu
XM_005261124.3:c.6218C>T	XP_005261181.1:p.Pro2073Leu
XM_011529593.1:c.6296C>T	XP_011527895.1:p.Pro2099Leu
XM_011529594.1:c.6266C>T	XP_011527896.1:p.Pro2089Leu
XM_005261124.5:c.6218C>T	XP_005261181.1:p.Pro2073Leu
XM_011529594.3:c.6266C>T	XP_011527896.1:p.Pro2089Leu
XM_017028362.2:c.6185C>T	XP_016883851.1:p.Pro2062Leu
XM_017028363.1:c.5864C>T	XP_016883852.1:p.Pro1955Leu
XM_024452082.1:c.5102C>T	XP_024307850.1:p.Pro1701Leu
XM_024452083.1:c.3998C>T	XP_024307851.1:p.Pro1333Leu
NM_006031.6:c.6185C>T MANE Select	NP_006022.3:p.Pro2062Leu
NM_001315529.2:c.5831C>T	NP_001302458.1:p.Pro1944Leu