Canonical Allele Identifier: CA324815
Community Standard Title: NM_033109.5(PNPT1):c.2014-3C>G
Gene: PNPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55643216G>C , CM000664.2:g.55643216G>C GRCh38
NC_000002.11:g.55870351G>C , CM000664.1:g.55870351G>C GRCh37
NC_000002.10:g.55723855G>C NCBI36
NG_033012.1:g.55695C>G

Transcript Alleles

HGVS Amino-acid Change
NM_033109.5:c.2014-3C>G MANE Select NP_149100.2:n.2014-3C>G
ENST00000447944.7:c.2014-3C>G MANE Select ENSP00000400646.2:n.2014-3C>G
NM_033109.4:c.2014-3C>G NP_149100.2:n.2014-3C>G
ENST00000260604.8:c.*1556-3C>G ENSP00000260604.4:n.*1556-3C>G
ENST00000415374.5:c.2014-3C>G ENSP00000393953.1:n.2014-3C>G
ENST00000447944.6:c.2014-3C>G ENSP00000400646.2:n.2014-3C>G
ENST00000481066.1:n.1076-3C>G
XM_005264629.1:c.1774-3C>G XP_005264686.1:n.1774-3C>G
XM_005264629.2:c.1774-3C>G XP_005264686.1:n.1774-3C>G
XM_017005172.1:c.1774-3C>G XP_016860661.1:n.1774-3C>G