Canonical Allele Identifier: CA1252405648
Gene: PNPT1 HGNC NCBI

Linked Data

dbSNP Id: rs905134943

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55680769G>C , CM000664.2:g.55680769G>C GRCh38
NC_000002.11:g.55907904G>C , CM000664.1:g.55907904G>C GRCh37
NC_000002.10:g.55761408G>C NCBI36
NG_033012.1:g.18142C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000447944.7:c.518-10C>G MANE Select ENSP00000400646.2:n.518-10C>G
ENST00000260604.8:c.*63C>G ENSP00000260604.4:n.*63C>G
ENST00000415374.5:c.518-10C>G ENSP00000393953.1:n.518-10C>G
ENST00000429805.1:c.*166-10C>G ENSP00000411994.1:n.*166-10C>G
ENST00000447944.6:c.518-10C>G ENSP00000400646.2:n.518-10C>G
NM_033109.4:c.518-10C>G NP_149100.2:n.518-10C>G
XM_005264629.1:c.278-10C>G XP_005264686.1:n.278-10C>G
XM_011533142.1:c.518-10C>G XP_011531444.1:n.518-10C>G
XM_005264629.2:c.278-10C>G XP_005264686.1:n.278-10C>G
XM_017005172.1:c.278-10C>G XP_016860661.1:n.278-10C>G
XR_001739010.1:n.548-10C>G
NM_033109.5:c.518-10C>G MANE Select NP_149100.2:n.518-10C>G