Canonical Allele Identifier: CA346923783

Gene: PNPT1

Linked Data

• MyVariant Identifiers: chr2:g.55870321C>T (hg19) ; chr2:g.55643186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55643186C>T , CM000664.2:g.55643186C>T	GRCh38
NC_000002.11:g.55870321C>T , CM000664.1:g.55870321C>T	GRCh37
NC_000002.10:g.55723825C>T	NCBI36
NG_033012.1:g.55725G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.2041G>A MANE Select	ENSP00000400646.2:p.Val681Ile
ENST00000260604.8:c.*1583G>A	ENSP00000260604.4:n.*1583G>A
ENST00000415374.5:c.2041G>A	ENSP00000393953.1:p.Val681Ile
ENST00000447944.6:c.2041G>A	ENSP00000400646.2:p.Val681Ile
ENST00000481066.1:n.1103G>A
NM_033109.4:c.2041G>A	NP_149100.2:p.Val681Ile
XM_005264629.1:c.1801G>A	XP_005264686.1:p.Val601Ile
XM_005264629.2:c.1801G>A	XP_005264686.1:p.Val601Ile
XM_017005172.1:c.1801G>A	XP_016860661.1:p.Val601Ile
NM_033109.5:c.2041G>A MANE Select	NP_149100.2:p.Val681Ile