Canonical Allele Identifier: CA1252384177

Gene: PNPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55643080T= , CM000664.2:g.55643080T=	GRCh38
NC_000002.11:g.55870215T= , CM000664.1:g.55870215T=	GRCh37
NC_000002.10:g.55723719T=	NCBI36
NG_033012.1:g.55831A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.2069+78A= MANE Select	ENSP00000400646.2:n.2069+78A=
ENST00000260604.8:c.*1611+78A=	ENSP00000260604.4:n.*1611+78A=
ENST00000415374.5:c.2069+78A=	ENSP00000393953.1:n.2069+78A=
ENST00000447944.6:c.2069+78A=	ENSP00000400646.2:n.2069+78A=
ENST00000481066.1:n.1131+78A=
NM_033109.4:c.2069+78A=	NP_149100.2:n.2069+78A=
XM_005264629.1:c.1829+78A=	XP_005264686.1:n.1829+78A=
XM_005264629.2:c.1829+78A=	XP_005264686.1:n.1829+78A=
XM_017005172.1:c.1829+78A=	XP_016860661.1:n.1829+78A=
NM_033109.5:c.2069+78A= MANE Select	NP_149100.2:n.2069+78A=