Canonical Allele Identifier: CA2392665033

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46411741G= , CM000683.2:g.46411741G=	GRCh38
NC_000021.8:g.47831655G= , CM000683.1:g.47831655G=	GRCh37
NC_000021.7:g.46656083G=	NCBI36
NG_008961.1:g.92620G=
NG_008961.2:g.92620G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695527.1:n.13G=
ENST00000695558.1:c.5701G=	ENSP00000512015.1:p.Glu1901=
ENST00000703224.1:c.*4911G=	ENSP00000515242.1:n.*4911G=
ENST00000359568.10:c.5668G= MANE Select	ENSP00000352572.5:p.Glu1890=
ENST00000359568.9:c.5668G=	ENSP00000352572.5:p.Glu1890=
ENST00000480896.5:n.5937G=
NM_001315529.1:c.5314G=	NP_001302458.1:p.Glu1772=
NM_006031.5:c.5668G=	NP_006022.3:p.Glu1890=
XM_005261124.3:c.5701G=	XP_005261181.1:p.Glu1901=
XM_011529593.1:c.5779G=	XP_011527895.1:p.Glu1927=
XM_011529594.1:c.5749G=	XP_011527896.1:p.Glu1917=
XM_005261124.5:c.5701G=	XP_005261181.1:p.Glu1901=
XM_011529594.3:c.5749G=	XP_011527896.1:p.Glu1917=
XM_017028362.2:c.5668G=	XP_016883851.1:p.Glu1890=
XM_017028363.1:c.5347G=	XP_016883852.1:p.Glu1783=
XM_024452082.1:c.4585G=	XP_024307850.1:p.Glu1529=
XM_024452083.1:c.3481G=	XP_024307851.1:p.Glu1161=
NM_006031.6:c.5668G= MANE Select	NP_006022.3:p.Glu1890=
NM_001315529.2:c.5314G=	NP_001302458.1:p.Glu1772=