Canonical Allele Identifier: CA770363019

Gene: PNPT1

Linked Data

• dbSNP Id: rs1357794523
• gnomAD v3: 2-55680967-A-T
• gnomAD v4: 2-55680967-A-T
• MyVariant Identifiers: chr2:g.55908102A>T (hg19) ; chr2:g.55680967A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.55680967A>T , CM000664.2:g.55680967A>T	GRCh38
NC_000002.11:g.55908102A>T , CM000664.1:g.55908102A>T	GRCh37
NC_000002.10:g.55761606A>T	NCBI36
NG_033012.1:g.17944T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447944.7:c.454-49T>A MANE Select	ENSP00000400646.2:n.454-49T>A
ENST00000260604.8:c.454-49T>A	ENSP00000260604.4:n.454-49T>A
ENST00000415374.5:c.454-49T>A	ENSP00000393953.1:n.454-49T>A
ENST00000429805.1:c.*102-49T>A	ENSP00000411994.1:n.*102-49T>A
ENST00000447944.6:c.454-49T>A	ENSP00000400646.2:n.454-49T>A
NM_033109.4:c.454-49T>A	NP_149100.2:n.454-49T>A
XM_005264629.1:c.214-49T>A	XP_005264686.1:n.214-49T>A
XM_011533142.1:c.454-49T>A	XP_011531444.1:n.454-49T>A
XM_005264629.2:c.214-49T>A	XP_005264686.1:n.214-49T>A
XM_017005172.1:c.214-49T>A	XP_016860661.1:n.214-49T>A
XR_001739010.1:n.484-49T>A
NM_033109.5:c.454-49T>A MANE Select	NP_149100.2:n.454-49T>A