Canonical Allele Identifier: CA1252398331

Gene: PNPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55666942T= , CM000664.2:g.55666942T=	GRCh38
NC_000002.11:g.55894077T= , CM000664.1:g.55894077T=	GRCh37
NC_000002.10:g.55747581T=	NCBI36
NG_033012.1:g.31969A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.1176+49A= MANE Select	ENSP00000400646.2:n.1176+49A=
ENST00000260604.8:c.*731+49A=	ENSP00000260604.4:n.*731+49A=
ENST00000415374.5:c.1176+49A=	ENSP00000393953.1:n.1176+49A=
ENST00000415489.1:c.250+49A=
ENST00000447944.6:c.1176+49A=	ENSP00000400646.2:n.1176+49A=
NM_033109.4:c.1176+49A=	NP_149100.2:n.1176+49A=
XM_005264629.1:c.936+49A=	XP_005264686.1:n.936+49A=
XM_011533142.1:c.1176+49A=	XP_011531444.1:n.1176+49A=
XM_005264629.2:c.936+49A=	XP_005264686.1:n.936+49A=
XM_017005172.1:c.936+49A=	XP_016860661.1:n.936+49A=
XR_001739010.1:n.1206+49A=
NM_033109.5:c.1176+49A= MANE Select	NP_149100.2:n.1176+49A=