Canonical Allele Identifier: CA346923771

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55870316A>T (hg19) ; chr2:g.55643181A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55643181A>T , CM000664.2:g.55643181A>T	GRCh38
NC_000002.11:g.55870316A>T , CM000664.1:g.55870316A>T	GRCh37
NC_000002.10:g.55723820A>T	NCBI36
NG_033012.1:g.55730T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.2046T>A MANE Select	ENSP00000400646.2:p.Tyr682Ter
ENST00000260604.8:c.*1588T>A	ENSP00000260604.4:n.*1588T>A
ENST00000415374.5:c.2046T>A	ENSP00000393953.1:p.Tyr682Ter
ENST00000447944.6:c.2046T>A	ENSP00000400646.2:p.Tyr682Ter
ENST00000481066.1:n.1108T>A
NM_033109.4:c.2046T>A	NP_149100.2:p.Tyr682Ter
XM_005264629.1:c.1806T>A	XP_005264686.1:p.Tyr602Ter
XM_005264629.2:c.1806T>A	XP_005264686.1:p.Tyr602Ter
XM_017005172.1:c.1806T>A	XP_016860661.1:p.Tyr602Ter
NM_033109.5:c.2046T>A MANE Select	NP_149100.2:p.Tyr682Ter