Canonical Allele Identifier: CA532795581

Gene: PNPT1

Linked Data

• dbSNP Id: rs1009751456
• gnomAD v2: 2-55899579-G-T
• gnomAD v3: 2-55672444-G-T
• gnomAD v4: 2-55672444-G-T
• MyVariant Identifiers: chr2:g.55899579G>T (hg19) ; chr2:g.55672444G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55672444G>T , CM000664.2:g.55672444G>T	GRCh38
NC_000002.11:g.55899579G>T , CM000664.1:g.55899579G>T	GRCh37
NC_000002.10:g.55753083G>T	NCBI36
NG_033012.1:g.26467C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.867-398C>A MANE Select	ENSP00000400646.2:n.867-398C>A
ENST00000260604.8:c.*422-398C>A	ENSP00000260604.4:n.*422-398C>A
ENST00000415374.5:c.867-398C>A	ENSP00000393953.1:n.867-398C>A
ENST00000447944.6:c.867-398C>A	ENSP00000400646.2:n.867-398C>A
NM_033109.4:c.867-398C>A	NP_149100.2:n.867-398C>A
XM_005264629.1:c.627-398C>A	XP_005264686.1:n.627-398C>A
XM_011533142.1:c.867-398C>A	XP_011531444.1:n.867-398C>A
XM_005264629.2:c.627-398C>A	XP_005264686.1:n.627-398C>A
XM_017005172.1:c.627-398C>A	XP_016860661.1:n.627-398C>A
XR_001739010.1:n.897-398C>A
NM_033109.5:c.867-398C>A MANE Select	NP_149100.2:n.867-398C>A