Canonical Allele Identifier: CA346928719

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55894196T>G (hg19) ; chr2:g.55667061T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55667061T>G , CM000664.2:g.55667061T>G	GRCh38
NC_000002.11:g.55894196T>G , CM000664.1:g.55894196T>G	GRCh37
NC_000002.10:g.55747700T>G	NCBI36
NG_033012.1:g.31850A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.1106A>C MANE Select	ENSP00000400646.2:p.Asn369Thr
ENST00000260604.8:c.*661A>C	ENSP00000260604.4:n.*661A>C
ENST00000415374.5:c.1106A>C	ENSP00000393953.1:p.Asn369Thr
ENST00000415489.1:c.180A>C
ENST00000447944.6:c.1106A>C	ENSP00000400646.2:p.Asn369Thr
NM_033109.4:c.1106A>C	NP_149100.2:p.Asn369Thr
XM_005264629.1:c.866A>C	XP_005264686.1:p.Asn289Thr
XM_011533142.1:c.1106A>C	XP_011531444.1:p.Asn369Thr
XM_005264629.2:c.866A>C	XP_005264686.1:p.Asn289Thr
XM_017005172.1:c.866A>C	XP_016860661.1:p.Asn289Thr
XR_001739010.1:n.1136A>C
NM_033109.5:c.1106A>C MANE Select	NP_149100.2:p.Asn369Thr