Canonical Allele Identifier: CA2392665085

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46411840C= , CM000683.2:g.46411840C=	GRCh38
NC_000021.8:g.47831754C= , CM000683.1:g.47831754C=	GRCh37
NC_000021.7:g.46656182C=	NCBI36
NG_008961.1:g.92719C=
NG_008961.2:g.92719C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695527.1:n.112C=
ENST00000695558.1:c.5800C=	ENSP00000512015.1:p.Arg1934=
ENST00000703224.1:c.*5010C=	ENSP00000515242.1:n.*5010C=
ENST00000359568.10:c.5767C= MANE Select	ENSP00000352572.5:p.Arg1923=
ENST00000359568.9:c.5767C=	ENSP00000352572.5:p.Arg1923=
ENST00000480896.5:n.6036C=
NM_001315529.1:c.5413C=	NP_001302458.1:p.Arg1805=
NM_006031.5:c.5767C=	NP_006022.3:p.Arg1923=
XM_005261124.3:c.5800C=	XP_005261181.1:p.Arg1934=
XM_011529593.1:c.5878C=	XP_011527895.1:p.Arg1960=
XM_011529594.1:c.5848C=	XP_011527896.1:p.Arg1950=
XM_005261124.5:c.5800C=	XP_005261181.1:p.Arg1934=
XM_011529594.3:c.5848C=	XP_011527896.1:p.Arg1950=
XM_017028362.2:c.5767C=	XP_016883851.1:p.Arg1923=
XM_017028363.1:c.5446C=	XP_016883852.1:p.Arg1816=
XM_024452082.1:c.4684C=	XP_024307850.1:p.Arg1562=
XM_024452083.1:c.3580C=	XP_024307851.1:p.Arg1194=
NM_006031.6:c.5767C= MANE Select	NP_006022.3:p.Arg1923=
NM_001315529.2:c.5413C=	NP_001302458.1:p.Arg1805=