Canonical Allele Identifier: CA1252384214

Gene: PNPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55643114_55643116delinsTAA , CM000664.2:g.55643114_55643116delinsTAA	GRCh38
NC_000002.11:g.55870249_55870251delinsTAA , CM000664.1:g.55870249_55870251delinsTAA	GRCh37
NC_000002.10:g.55723753_55723755delinsTAA	NCBI36
NG_033012.1:g.55795_55797delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.2069+42_2069+44delinsTTA MANE Select	ENSP00000400646.2:n.2069+42_2069+44delinsTTA
ENST00000260604.8:c.*1611+42_*1611+44delinsTTA	ENSP00000260604.4:n.*1611+42_*1611+44delinsTTA
ENST00000415374.5:c.2069+42_2069+44delinsTTA	ENSP00000393953.1:n.2069+42_2069+44delinsTTA
ENST00000447944.6:c.2069+42_2069+44delinsTTA	ENSP00000400646.2:n.2069+42_2069+44delinsTTA
ENST00000481066.1:n.1131+42_1131+44delinsTTA
NM_033109.4:c.2069+42_2069+44delinsTTA	NP_149100.2:n.2069+42_2069+44delinsTTA
XM_005264629.1:c.1829+42_1829+44delinsTTA	XP_005264686.1:n.1829+42_1829+44delinsTTA
XM_005264629.2:c.1829+42_1829+44delinsTTA	XP_005264686.1:n.1829+42_1829+44delinsTTA
XM_017005172.1:c.1829+42_1829+44delinsTTA	XP_016860661.1:n.1829+42_1829+44delinsTTA
NM_033109.5:c.2069+42_2069+44delinsTTA MANE Select	NP_149100.2:n.2069+42_2069+44delinsTTA