Canonical Allele Identifier: CA1030920561

Gene: PNPT1

Linked Data

• dbSNP Id: rs1696938731
• gnomAD v3: 2-55672242-TC-T
• gnomAD v4: 2-55672242-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55672243del , CM000664.2:g.55672243del	GRCh38
NC_000002.11:g.55899378del , CM000664.1:g.55899378del	GRCh37
NC_000002.10:g.55752882del	NCBI36
NG_033012.1:g.26668del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.867-197del MANE Select	ENSP00000400646.2:n.867-197del
ENST00000260604.8:c.*422-197del	ENSP00000260604.4:n.*422-197del
ENST00000415374.5:c.867-197del	ENSP00000393953.1:n.867-197del
ENST00000447944.6:c.867-197del	ENSP00000400646.2:n.867-197del
NM_033109.4:c.867-197del	NP_149100.2:n.867-197del
XM_005264629.1:c.627-197del	XP_005264686.1:n.627-197del
XM_011533142.1:c.867-197del	XP_011531444.1:n.867-197del
XM_005264629.2:c.627-197del	XP_005264686.1:n.627-197del
XM_017005172.1:c.627-197del	XP_016860661.1:n.627-197del
XR_001739010.1:n.897-197del
NM_033109.5:c.867-197del MANE Select	NP_149100.2:n.867-197del