Canonical Allele Identifier: CA346928580

Gene: PNPT1

Linked Data

• dbSNP Id: rs1338957358
• gnomAD v3: 2-55667002-C-T
• gnomAD v4: 2-55667002-C-T
• MyVariant Identifiers: chr2:g.55894137C>T (hg19) ; chr2:g.55667002C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55667002C>T , CM000664.2:g.55667002C>T	GRCh38
NC_000002.11:g.55894137C>T , CM000664.1:g.55894137C>T	GRCh37
NC_000002.10:g.55747641C>T	NCBI36
NG_033012.1:g.31909G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.1165G>A MANE Select	ENSP00000400646.2:p.Gly389Arg
ENST00000260604.8:c.*720G>A	ENSP00000260604.4:n.*720G>A
ENST00000415374.5:c.1165G>A	ENSP00000393953.1:p.Gly389Arg
ENST00000415489.1:c.239G>A
ENST00000447944.6:c.1165G>A	ENSP00000400646.2:p.Gly389Arg
NM_033109.4:c.1165G>A	NP_149100.2:p.Gly389Arg
XM_005264629.1:c.925G>A	XP_005264686.1:p.Gly309Arg
XM_011533142.1:c.1165G>A	XP_011531444.1:p.Gly389Arg
XM_005264629.2:c.925G>A	XP_005264686.1:p.Gly309Arg
XM_017005172.1:c.925G>A	XP_016860661.1:p.Gly309Arg
XR_001739010.1:n.1195G>A
NM_033109.5:c.1165G>A MANE Select	NP_149100.2:p.Gly389Arg