Canonical Allele Identifier: CA2392665107

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46411884C= , CM000683.2:g.46411884C=	GRCh38
NC_000021.8:g.47831798C= , CM000683.1:g.47831798C=	GRCh37
NC_000021.7:g.46656226C=	NCBI36
NG_008961.1:g.92763C=
NG_008961.2:g.92763C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695527.1:n.156C=
ENST00000695558.1:c.5844C=	ENSP00000512015.1:p.His1948=
ENST00000703224.1:c.*5054C=	ENSP00000515242.1:n.*5054C=
ENST00000359568.10:c.5811C= MANE Select	ENSP00000352572.5:p.His1937=
ENST00000359568.9:c.5811C=	ENSP00000352572.5:p.His1937=
ENST00000480896.5:n.6080C=
NM_001315529.1:c.5457C=	NP_001302458.1:p.His1819=
NM_006031.5:c.5811C=	NP_006022.3:p.His1937=
XM_005261124.3:c.5844C=	XP_005261181.1:p.His1948=
XM_011529593.1:c.5922C=	XP_011527895.1:p.His1974=
XM_011529594.1:c.5892C=	XP_011527896.1:p.His1964=
XM_005261124.5:c.5844C=	XP_005261181.1:p.His1948=
XM_011529594.3:c.5892C=	XP_011527896.1:p.His1964=
XM_017028362.2:c.5811C=	XP_016883851.1:p.His1937=
XM_017028363.1:c.5490C=	XP_016883852.1:p.His1830=
XM_024452082.1:c.4728C=	XP_024307850.1:p.His1576=
XM_024452083.1:c.3624C=	XP_024307851.1:p.His1208=
NM_006031.6:c.5811C= MANE Select	NP_006022.3:p.His1937=
NM_001315529.2:c.5457C=	NP_001302458.1:p.His1819=