Canonical Allele Identifier: CA426175446

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55908000T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55680865T>A , CM000664.2:g.55680865T>A	GRCh38
NC_000002.11:g.55908000T>A , CM000664.1:g.55908000T>A	GRCh37
NC_000002.10:g.55761504T>A	NCBI36
NG_033012.1:g.18046A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.507A>T MANE Select	ENSP00000400646.2:p.Ala169=
ENST00000260604.8:c.507A>T	ENSP00000260604.4:p.Ala169=
ENST00000415374.5:c.507A>T	ENSP00000393953.1:p.Ala169=
ENST00000429805.1:c.*155A>T	ENSP00000411994.1:n.*155A>T
ENST00000447944.6:c.507A>T	ENSP00000400646.2:p.Ala169=
NM_033109.4:c.507A>T	NP_149100.2:p.Ala169=
XM_005264629.1:c.267A>T	XP_005264686.1:p.Ala89=
XM_011533142.1:c.507A>T	XP_011531444.1:p.Ala169=
XM_005264629.2:c.267A>T	XP_005264686.1:p.Ala89=
XM_017005172.1:c.267A>T	XP_016860661.1:p.Ala89=
XR_001739010.1:n.537A>T
NM_033109.5:c.507A>T MANE Select	NP_149100.2:p.Ala169=