Canonical Allele Identifier: CA2655021753

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46389189C>T , CM000683.2:g.46389189C>T	GRCh38
NC_000021.8:g.47809104C>T , CM000683.1:g.47809104C>T	GRCh37
NC_000021.7:g.46633532C>T	NCBI36
NG_008961.1:g.70069C>T
NG_008961.2:g.70068C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006031.6:c.3608-10C>T MANE Select	NP_006022.3:n.3608-10C>T
ENST00000359568.10:c.3608-10C>T MANE Select	ENSP00000352572.5:n.3608-10C>T
NM_001315529.1:c.3254-10C>T	NP_001302458.1:n.3254-10C>T
NM_001315529.2:c.3254-10C>T	NP_001302458.1:n.3254-10C>T
NM_006031.5:c.3608-10C>T	NP_006022.3:n.3608-10C>T
ENST00000359568.9:c.3608-10C>T	ENSP00000352572.5:n.3608-10C>T
ENST00000466474.6:c.*2104-10C>T	ENSP00000511987.1:n.*2104-10C>T
ENST00000480896.5:n.3877-10C>T
ENST00000695525.1:n.3694-10C>T
ENST00000695558.1:c.3608-10C>T	ENSP00000512015.1:n.3608-10C>T
ENST00000703224.1:c.*2851-10C>T	ENSP00000515242.1:n.*2851-10C>T
XM_005261124.3:c.3608-10C>T	XP_005261181.1:n.3608-10C>T
XM_005261124.5:c.3608-10C>T	XP_005261181.1:n.3608-10C>T
XM_011529593.1:c.3689-10C>T	XP_011527895.1:n.3689-10C>T
XM_011529594.1:c.3689-10C>T	XP_011527896.1:n.3689-10C>T
XM_011529594.3:c.3689-10C>T	XP_011527896.1:n.3689-10C>T
XM_017028362.2:c.3608-10C>T	XP_016883851.1:n.3608-10C>T
XM_017028363.1:c.3254-10C>T	XP_016883852.1:n.3254-10C>T
XM_024452082.1:c.2492-10C>T	XP_024307850.1:n.2492-10C>T
XM_024452083.1:c.1388-10C>T	XP_024307851.1:n.1388-10C>T