Canonical Allele Identifier: CA2392673255

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46425921C= , CM000683.2:g.46425921C=	GRCh38
NC_000021.8:g.47845835C= , CM000683.1:g.47845835C=	GRCh37
NC_000021.7:g.46670263C=	NCBI36
NG_008961.1:g.106800C=
NG_008961.2:g.106800C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006031.6:c.7270C= MANE Select	NP_006022.3:p.Arg2424=
ENST00000359568.10:c.7270C= MANE Select	ENSP00000352572.5:p.Arg2424=
NM_001315529.1:c.6916C=	NP_001302458.1:p.Arg2306=
NM_001315529.2:c.6916C=	NP_001302458.1:p.Arg2306=
NM_006031.5:c.7270C=	NP_006022.3:p.Arg2424=
ENST00000359568.9:c.7270C=	ENSP00000352572.5:p.Arg2424=
ENST00000418394.2:c.89C=
ENST00000480896.5:n.7539C=
ENST00000695527.1:n.1615C=
ENST00000695528.1:c.1354-1701C=	ENSP00000511990.1:n.1354-1701C=
ENST00000695529.1:n.1354-1701C=
ENST00000695530.1:c.89C=
ENST00000695558.1:c.7303C=	ENSP00000512015.1:p.Arg2435=
ENST00000703224.1:c.*6513C=	ENSP00000515242.1:n.*6513C=
XM_005261124.3:c.7303C=	XP_005261181.1:p.Arg2435=
XM_005261124.5:c.7303C=	XP_005261181.1:p.Arg2435=
XM_011529593.1:c.7381C=	XP_011527895.1:p.Arg2461=
XM_011529594.1:c.7351C=	XP_011527896.1:p.Arg2451=
XM_011529594.3:c.7351C=	XP_011527896.1:p.Arg2451=
XM_017028362.2:c.7270C=	XP_016883851.1:p.Arg2424=
XM_017028363.1:c.6949C=	XP_016883852.1:p.Arg2317=
XM_024452082.1:c.6187C=	XP_024307850.1:p.Arg2063=
XM_024452083.1:c.5083C=	XP_024307851.1:p.Arg1695=