Canonical Allele Identifier: CA2392665034

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46411746G= , CM000683.2:g.46411746G=	GRCh38
NC_000021.8:g.47831660G= , CM000683.1:g.47831660G=	GRCh37
NC_000021.7:g.46656088G=	NCBI36
NG_008961.1:g.92625G=
NG_008961.2:g.92625G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695527.1:n.18G=
ENST00000695558.1:c.5706G=	ENSP00000512015.1:p.Leu1902=
ENST00000703224.1:c.*4916G=	ENSP00000515242.1:n.*4916G=
ENST00000359568.10:c.5673G= MANE Select	ENSP00000352572.5:p.Leu1891=
ENST00000359568.9:c.5673G=	ENSP00000352572.5:p.Leu1891=
ENST00000480896.5:n.5942G=
NM_001315529.1:c.5319G=	NP_001302458.1:p.Leu1773=
NM_006031.5:c.5673G=	NP_006022.3:p.Leu1891=
XM_005261124.3:c.5706G=	XP_005261181.1:p.Leu1902=
XM_011529593.1:c.5784G=	XP_011527895.1:p.Leu1928=
XM_011529594.1:c.5754G=	XP_011527896.1:p.Leu1918=
XM_005261124.5:c.5706G=	XP_005261181.1:p.Leu1902=
XM_011529594.3:c.5754G=	XP_011527896.1:p.Leu1918=
XM_017028362.2:c.5673G=	XP_016883851.1:p.Leu1891=
XM_017028363.1:c.5352G=	XP_016883852.1:p.Leu1784=
XM_024452082.1:c.4590G=	XP_024307850.1:p.Leu1530=
XM_024452083.1:c.3486G=	XP_024307851.1:p.Leu1162=
NM_006031.6:c.5673G= MANE Select	NP_006022.3:p.Leu1891=
NM_001315529.2:c.5319G=	NP_001302458.1:p.Leu1773=