Canonical Allele Identifier: CA1252387837

Gene: PNPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55647258C= , CM000664.2:g.55647258C=	GRCh38
NC_000002.11:g.55874393C= , CM000664.1:g.55874393C=	GRCh37
NC_000002.10:g.55727897C=	NCBI36
NG_033012.1:g.51653G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000447944.7:c.1602+89G= MANE Select	ENSP00000400646.2:n.1602+89G=
ENST00000260604.8:c.*1157+89G=	ENSP00000260604.4:n.*1157+89G=
ENST00000415374.5:c.1602+89G=	ENSP00000393953.1:n.1602+89G=
ENST00000447944.6:c.1602+89G=	ENSP00000400646.2:n.1602+89G=
ENST00000481066.1:n.36+89G=
NM_033109.4:c.1602+89G=	NP_149100.2:n.1602+89G=
XM_005264629.1:c.1362+89G=	XP_005264686.1:n.1362+89G=
XM_005264629.2:c.1362+89G=	XP_005264686.1:n.1362+89G=
XM_017005172.1:c.1362+89G=	XP_016860661.1:n.1362+89G=
XR_001739010.1:n.1679+89G=
NM_033109.5:c.1602+89G= MANE Select	NP_149100.2:n.1602+89G=