Canonical Allele Identifier: CA2392665125

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46411921C= , CM000683.2:g.46411921C=	GRCh38
NC_000021.8:g.47831835C= , CM000683.1:g.47831835C=	GRCh37
NC_000021.7:g.46656263C=	NCBI36
NG_008961.1:g.92800C=
NG_008961.2:g.92800C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695527.1:n.193C=
ENST00000695528.1:c.22C=	ENSP00000511990.1:p.Arg8=
ENST00000695529.1:n.22C=
ENST00000695558.1:c.5881C=	ENSP00000512015.1:p.Arg1961=
ENST00000703224.1:c.*5091C=	ENSP00000515242.1:n.*5091C=
ENST00000359568.10:c.5848C= MANE Select	ENSP00000352572.5:p.Arg1950=
ENST00000359568.9:c.5848C=	ENSP00000352572.5:p.Arg1950=
ENST00000480896.5:n.6117C=
NM_001315529.1:c.5494C=	NP_001302458.1:p.Arg1832=
NM_006031.5:c.5848C=	NP_006022.3:p.Arg1950=
XM_005261124.3:c.5881C=	XP_005261181.1:p.Arg1961=
XM_011529593.1:c.5959C=	XP_011527895.1:p.Arg1987=
XM_011529594.1:c.5929C=	XP_011527896.1:p.Arg1977=
XM_005261124.5:c.5881C=	XP_005261181.1:p.Arg1961=
XM_011529594.3:c.5929C=	XP_011527896.1:p.Arg1977=
XM_017028362.2:c.5848C=	XP_016883851.1:p.Arg1950=
XM_017028363.1:c.5527C=	XP_016883852.1:p.Arg1843=
XM_024452082.1:c.4765C=	XP_024307850.1:p.Arg1589=
XM_024452083.1:c.3661C=	XP_024307851.1:p.Arg1221=
NM_006031.6:c.5848C= MANE Select	NP_006022.3:p.Arg1950=
NM_001315529.2:c.5494C=	NP_001302458.1:p.Arg1832=