Canonical Allele Identifier: CA1252398325

Gene: PNPT1

Linked Data

• dbSNP Id: rs1696749017
• gnomAD v4: 2-55666926-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55666926C>A , CM000664.2:g.55666926C>A	GRCh38
NC_000002.11:g.55894061C>A , CM000664.1:g.55894061C>A	GRCh37
NC_000002.10:g.55747565C>A	NCBI36
NG_033012.1:g.31985G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000447944.7:c.1176+65G>T MANE Select	ENSP00000400646.2:n.1176+65G>T
ENST00000260604.8:c.*731+65G>T	ENSP00000260604.4:n.*731+65G>T
ENST00000415374.5:c.1176+65G>T	ENSP00000393953.1:n.1176+65G>T
ENST00000415489.1:c.250+65G>T
ENST00000447944.6:c.1176+65G>T	ENSP00000400646.2:n.1176+65G>T
NM_033109.4:c.1176+65G>T	NP_149100.2:n.1176+65G>T
XM_005264629.1:c.936+65G>T	XP_005264686.1:n.936+65G>T
XM_011533142.1:c.1176+65G>T	XP_011531444.1:n.1176+65G>T
XM_005264629.2:c.936+65G>T	XP_005264686.1:n.936+65G>T
XM_017005172.1:c.936+65G>T	XP_016860661.1:n.936+65G>T
XR_001739010.1:n.1206+65G>T
NM_033109.5:c.1176+65G>T MANE Select	NP_149100.2:n.1176+65G>T