Canonical Allele Identifier: CA2695205328
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114521del , CM000667.2:g.140114521del GRCh38
NC_000005.9:g.139494106del , CM000667.1:g.139494106del GRCh37
NC_000005.8:g.139474290del NCBI36
NG_041813.1:g.5399del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.340del MANE Select ENSP00000332706.3:p.Leu114TrpfsTer?
ENST00000651386.1:c.340del ENSP00000499133.1:p.Leu114TrpfsTer?
ENST00000331327.4:c.340del ENSP00000332706.3:p.Leu114TrpfsTer?
NM_005859.4:c.340del NP_005850.1:p.Leu114TrpfsTer?
NM_005859.5:c.340del MANE Select NP_005850.1:p.Leu114TrpfsTer?