Canonical Allele Identifier: CA1252398367

Gene: PNPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55666996T= , CM000664.2:g.55666996T=	GRCh38
NC_000002.11:g.55894131T= , CM000664.1:g.55894131T=	GRCh37
NC_000002.10:g.55747635T=	NCBI36
NG_033012.1:g.31915A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.1171A= MANE Select	ENSP00000400646.2:p.Thr391=
ENST00000260604.8:c.*726A=	ENSP00000260604.4:n.*726A=
ENST00000415374.5:c.1171A=	ENSP00000393953.1:p.Thr391=
ENST00000415489.1:c.245A=
ENST00000447944.6:c.1171A=	ENSP00000400646.2:p.Thr391=
NM_033109.4:c.1171A=	NP_149100.2:p.Thr391=
XM_005264629.1:c.931A=	XP_005264686.1:p.Thr311=
XM_011533142.1:c.1171A=	XP_011531444.1:p.Thr391=
XM_005264629.2:c.931A=	XP_005264686.1:p.Thr311=
XM_017005172.1:c.931A=	XP_016860661.1:p.Thr311=
XR_001739010.1:n.1201A=
NM_033109.5:c.1171A= MANE Select	NP_149100.2:p.Thr391=