Canonical Allele Identifier: CA2392665038

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46411753G= , CM000683.2:g.46411753G=	GRCh38
NC_000021.8:g.47831667G= , CM000683.1:g.47831667G=	GRCh37
NC_000021.7:g.46656095G=	NCBI36
NG_008961.1:g.92632G=
NG_008961.2:g.92632G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695527.1:n.25G=
ENST00000695558.1:c.5713G=	ENSP00000512015.1:p.Val1905=
ENST00000703224.1:c.*4923G=	ENSP00000515242.1:n.*4923G=
ENST00000359568.10:c.5680G= MANE Select	ENSP00000352572.5:p.Val1894=
ENST00000359568.9:c.5680G=	ENSP00000352572.5:p.Val1894=
ENST00000480896.5:n.5949G=
NM_001315529.1:c.5326G=	NP_001302458.1:p.Val1776=
NM_006031.5:c.5680G=	NP_006022.3:p.Val1894=
XM_005261124.3:c.5713G=	XP_005261181.1:p.Val1905=
XM_011529593.1:c.5791G=	XP_011527895.1:p.Val1931=
XM_011529594.1:c.5761G=	XP_011527896.1:p.Val1921=
XM_005261124.5:c.5713G=	XP_005261181.1:p.Val1905=
XM_011529594.3:c.5761G=	XP_011527896.1:p.Val1921=
XM_017028362.2:c.5680G=	XP_016883851.1:p.Val1894=
XM_017028363.1:c.5359G=	XP_016883852.1:p.Val1787=
XM_024452082.1:c.4597G=	XP_024307850.1:p.Val1533=
XM_024452083.1:c.3493G=	XP_024307851.1:p.Val1165=
NM_006031.6:c.5680G= MANE Select	NP_006022.3:p.Val1894=
NM_001315529.2:c.5326G=	NP_001302458.1:p.Val1776=