Canonical Allele Identifier: CA1252405705

Gene: PNPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55680895T= , CM000664.2:g.55680895T=	GRCh38
NC_000002.11:g.55908030T= , CM000664.1:g.55908030T=	GRCh37
NC_000002.10:g.55761534T=	NCBI36
NG_033012.1:g.18016A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.477A= MANE Select	ENSP00000400646.2:p.Val159=
ENST00000260604.8:c.477A=	ENSP00000260604.4:p.Val159=
ENST00000415374.5:c.477A=	ENSP00000393953.1:p.Val159=
ENST00000429805.1:c.*125A=	ENSP00000411994.1:n.*125A=
ENST00000447944.6:c.477A=	ENSP00000400646.2:p.Val159=
NM_033109.4:c.477A=	NP_149100.2:p.Val159=
XM_005264629.1:c.237A=	XP_005264686.1:p.Val79=
XM_011533142.1:c.477A=	XP_011531444.1:p.Val159=
XM_005264629.2:c.237A=	XP_005264686.1:p.Val79=
XM_017005172.1:c.237A=	XP_016860661.1:p.Val79=
XR_001739010.1:n.507A=
NM_033109.5:c.477A= MANE Select	NP_149100.2:p.Val159=