Canonical Allele Identifier: CA2392665035

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46411750G= , CM000683.2:g.46411750G=	GRCh38
NC_000021.8:g.47831664G= , CM000683.1:g.47831664G=	GRCh37
NC_000021.7:g.46656092G=	NCBI36
NG_008961.1:g.92629G=
NG_008961.2:g.92629G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695527.1:n.22G=
ENST00000695558.1:c.5710G=	ENSP00000512015.1:p.Ala1904=
ENST00000703224.1:c.*4920G=	ENSP00000515242.1:n.*4920G=
ENST00000359568.10:c.5677G= MANE Select	ENSP00000352572.5:p.Ala1893=
ENST00000359568.9:c.5677G=	ENSP00000352572.5:p.Ala1893=
ENST00000480896.5:n.5946G=
NM_001315529.1:c.5323G=	NP_001302458.1:p.Ala1775=
NM_006031.5:c.5677G=	NP_006022.3:p.Ala1893=
XM_005261124.3:c.5710G=	XP_005261181.1:p.Ala1904=
XM_011529593.1:c.5788G=	XP_011527895.1:p.Ala1930=
XM_011529594.1:c.5758G=	XP_011527896.1:p.Ala1920=
XM_005261124.5:c.5710G=	XP_005261181.1:p.Ala1904=
XM_011529594.3:c.5758G=	XP_011527896.1:p.Ala1920=
XM_017028362.2:c.5677G=	XP_016883851.1:p.Ala1893=
XM_017028363.1:c.5356G=	XP_016883852.1:p.Ala1786=
XM_024452082.1:c.4594G=	XP_024307850.1:p.Ala1532=
XM_024452083.1:c.3490G=	XP_024307851.1:p.Ala1164=
NM_006031.6:c.5677G= MANE Select	NP_006022.3:p.Ala1893=
NM_001315529.2:c.5323G=	NP_001302458.1:p.Ala1775=