Canonical Allele Identifier: CA346938833

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55907895C>T (hg19) ; chr2:g.55680760C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55680760C>T , CM000664.2:g.55680760C>T	GRCh38
NC_000002.11:g.55907895C>T , CM000664.1:g.55907895C>T	GRCh37
NC_000002.10:g.55761399C>T	NCBI36
NG_033012.1:g.18151G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000447944.7:c.518-1G>A MANE Select	ENSP00000400646.2:n.518-1G>A
ENST00000260604.8:c.*72G>A	ENSP00000260604.4:n.*72G>A
ENST00000415374.5:c.518-1G>A	ENSP00000393953.1:n.518-1G>A
ENST00000429805.1:c.*166-1G>A	ENSP00000411994.1:n.*166-1G>A
ENST00000447944.6:c.518-1G>A	ENSP00000400646.2:n.518-1G>A
NM_033109.4:c.518-1G>A	NP_149100.2:n.518-1G>A
XM_005264629.1:c.278-1G>A	XP_005264686.1:n.278-1G>A
XM_011533142.1:c.518-1G>A	XP_011531444.1:n.518-1G>A
XM_005264629.2:c.278-1G>A	XP_005264686.1:n.278-1G>A
XM_017005172.1:c.278-1G>A	XP_016860661.1:n.278-1G>A
XR_001739010.1:n.548-1G>A
NM_033109.5:c.518-1G>A MANE Select	NP_149100.2:n.518-1G>A