Canonical Allele Identifier: CA346931985

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55899131T>A (hg19) ; chr2:g.55671996T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55671996T>A , CM000664.2:g.55671996T>A	GRCh38
NC_000002.11:g.55899131T>A , CM000664.1:g.55899131T>A	GRCh37
NC_000002.10:g.55752635T>A	NCBI36
NG_033012.1:g.26915A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.917A>T MANE Select	ENSP00000400646.2:p.Lys306Ile
ENST00000260604.8:c.*472A>T	ENSP00000260604.4:n.*472A>T
ENST00000415374.5:c.917A>T	ENSP00000393953.1:p.Lys306Ile
ENST00000447944.6:c.917A>T	ENSP00000400646.2:p.Lys306Ile
NM_033109.4:c.917A>T	NP_149100.2:p.Lys306Ile
XM_005264629.1:c.677A>T	XP_005264686.1:p.Lys226Ile
XM_011533142.1:c.917A>T	XP_011531444.1:p.Lys306Ile
XM_005264629.2:c.677A>T	XP_005264686.1:p.Lys226Ile
XM_017005172.1:c.677A>T	XP_016860661.1:p.Lys226Ile
XR_001739010.1:n.947A>T
NM_033109.5:c.917A>T MANE Select	NP_149100.2:p.Lys306Ile