Canonical Allele Identifier: CA2659132909
Gene: PNPT1 HGNC NCBI

Linked Data

gnomAD v4: 2-55666931-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55666931A>C , CM000664.2:g.55666931A>C GRCh38
NC_000002.11:g.55894066A>C , CM000664.1:g.55894066A>C GRCh37
NC_000002.10:g.55747570A>C NCBI36
NG_033012.1:g.31980T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000447944.7:c.1176+60T>G MANE Select ENSP00000400646.2:n.1176+60T>G
ENST00000260604.8:c.*731+60T>G ENSP00000260604.4:n.*731+60T>G
ENST00000415374.5:c.1176+60T>G ENSP00000393953.1:n.1176+60T>G
ENST00000415489.1:c.250+60T>G
ENST00000447944.6:c.1176+60T>G ENSP00000400646.2:n.1176+60T>G
NM_033109.4:c.1176+60T>G NP_149100.2:n.1176+60T>G
XM_005264629.1:c.936+60T>G XP_005264686.1:n.936+60T>G
XM_011533142.1:c.1176+60T>G XP_011531444.1:n.1176+60T>G
XM_005264629.2:c.936+60T>G XP_005264686.1:n.936+60T>G
XM_017005172.1:c.936+60T>G XP_016860661.1:n.936+60T>G
XR_001739010.1:n.1206+60T>G
NM_033109.5:c.1176+60T>G MANE Select NP_149100.2:n.1176+60T>G