Canonical Allele Identifier: CA1030920532

Gene: PNPT1

Linked Data

• dbSNP Id: rs1696936482
• gnomAD v3: 2-55672148-C-CT
• gnomAD v4: 2-55672148-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55672151dup , CM000664.2:g.55672151dup	GRCh38
NC_000002.11:g.55899286dup , CM000664.1:g.55899286dup	GRCh37
NC_000002.10:g.55752790dup	NCBI36
NG_033012.1:g.26762dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.867-103dup MANE Select	ENSP00000400646.2:n.867-103dup
ENST00000260604.8:c.*422-103dup	ENSP00000260604.4:n.*422-103dup
ENST00000415374.5:c.867-103dup	ENSP00000393953.1:n.867-103dup
ENST00000447944.6:c.867-103dup	ENSP00000400646.2:n.867-103dup
NM_033109.4:c.867-103dup	NP_149100.2:n.867-103dup
XM_005264629.1:c.627-103dup	XP_005264686.1:n.627-103dup
XM_011533142.1:c.867-103dup	XP_011531444.1:n.867-103dup
XM_005264629.2:c.627-103dup	XP_005264686.1:n.627-103dup
XM_017005172.1:c.627-103dup	XP_016860661.1:n.627-103dup
XR_001739010.1:n.897-103dup
NM_033109.5:c.867-103dup MANE Select	NP_149100.2:n.867-103dup