Canonical Allele Identifier: CA426171416

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55870307T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55643172T>G , CM000664.2:g.55643172T>G	GRCh38
NC_000002.11:g.55870307T>G , CM000664.1:g.55870307T>G	GRCh37
NC_000002.10:g.55723811T>G	NCBI36
NG_033012.1:g.55739A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.2055A>C MANE Select	ENSP00000400646.2:p.Thr685=
ENST00000260604.8:c.*1597A>C	ENSP00000260604.4:n.*1597A>C
ENST00000415374.5:c.2055A>C	ENSP00000393953.1:p.Thr685=
ENST00000447944.6:c.2055A>C	ENSP00000400646.2:p.Thr685=
ENST00000481066.1:n.1117A>C
NM_033109.4:c.2055A>C	NP_149100.2:p.Thr685=
XM_005264629.1:c.1815A>C	XP_005264686.1:p.Thr605=
XM_005264629.2:c.1815A>C	XP_005264686.1:p.Thr605=
XM_017005172.1:c.1815A>C	XP_016860661.1:p.Thr605=
NM_033109.5:c.2055A>C MANE Select	NP_149100.2:p.Thr685=