Canonical Allele Identifier: CA426173189

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55883297T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55656162T>G , CM000664.2:g.55656162T>G	GRCh38
NC_000002.11:g.55883297T>G , CM000664.1:g.55883297T>G	GRCh37
NC_000002.10:g.55736801T>G	NCBI36
NG_033012.1:g.42749A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000447944.7:c.1410A>C MANE Select	ENSP00000400646.2:p.Ile470=
ENST00000260604.8:c.*965A>C	ENSP00000260604.4:n.*965A>C
ENST00000415374.5:c.1410A>C	ENSP00000393953.1:p.Ile470=
ENST00000415489.1:c.417A>C
ENST00000447944.6:c.1410A>C	ENSP00000400646.2:p.Ile470=
NM_033109.4:c.1410A>C	NP_149100.2:p.Ile470=
XM_005264629.1:c.1170A>C	XP_005264686.1:p.Ile390=
XM_011533142.1:c.1410A>C	XP_011531444.1:p.Ile470=
XM_005264629.2:c.1170A>C	XP_005264686.1:p.Ile390=
XM_017005172.1:c.1170A>C	XP_016860661.1:p.Ile390=
XR_001739010.1:n.1440A>C
NM_033109.5:c.1410A>C MANE Select	NP_149100.2:p.Ile470=