Canonical Allele Identifier: CA1252398314
Gene: PNPT1 HGNC NCBI

Linked Data

dbSNP Id: rs1696748336
gnomAD v4: 2-55666895-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55666895T>C , CM000664.2:g.55666895T>C GRCh38
NC_000002.11:g.55894030T>C , CM000664.1:g.55894030T>C GRCh37
NC_000002.10:g.55747534T>C NCBI36
NG_033012.1:g.32016A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000447944.7:c.1176+96A>G MANE Select ENSP00000400646.2:n.1176+96A>G
ENST00000260604.8:c.*731+96A>G ENSP00000260604.4:n.*731+96A>G
ENST00000415374.5:c.1176+96A>G ENSP00000393953.1:n.1176+96A>G
ENST00000415489.1:c.250+96A>G
ENST00000447944.6:c.1176+96A>G ENSP00000400646.2:n.1176+96A>G
NM_033109.4:c.1176+96A>G NP_149100.2:n.1176+96A>G
XM_005264629.1:c.936+96A>G XP_005264686.1:n.936+96A>G
XM_011533142.1:c.1176+96A>G XP_011531444.1:n.1176+96A>G
XM_005264629.2:c.936+96A>G XP_005264686.1:n.936+96A>G
XM_017005172.1:c.936+96A>G XP_016860661.1:n.936+96A>G
XR_001739010.1:n.1206+96A>G
NM_033109.5:c.1176+96A>G MANE Select NP_149100.2:n.1176+96A>G