Canonical Allele Identifier: CA2659134739

Gene: PNPT1

Linked Data

• gnomAD v4: 2-55684875-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55684875G>T , CM000664.2:g.55684875G>T	GRCh38
NC_000002.11:g.55912010G>T , CM000664.1:g.55912010G>T	GRCh37
NC_000002.10:g.55765514G>T	NCBI36
NG_033012.1:g.14036C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000447944.7:c.403+68C>A MANE Select	ENSP00000400646.2:n.403+68C>A
ENST00000260604.8:c.403+68C>A	ENSP00000260604.4:n.403+68C>A
ENST00000415374.5:c.403+68C>A	ENSP00000393953.1:n.403+68C>A
ENST00000429805.1:c.*51+68C>A	ENSP00000411994.1:n.*51+68C>A
ENST00000447944.6:c.403+68C>A	ENSP00000400646.2:n.403+68C>A
NM_033109.4:c.403+68C>A	NP_149100.2:n.403+68C>A
XM_005264629.1:c.163+68C>A	XP_005264686.1:n.163+68C>A
XM_011533142.1:c.403+68C>A	XP_011531444.1:n.403+68C>A
XM_005264629.2:c.163+68C>A	XP_005264686.1:n.163+68C>A
XM_017005172.1:c.163+68C>A	XP_016860661.1:n.163+68C>A
XR_001739010.1:n.433+68C>A
NM_033109.5:c.403+68C>A MANE Select	NP_149100.2:n.403+68C>A