Canonical Allele Identifier: CA2675565395
Gene: PURA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114216del , CM000667.2:g.140114216del GRCh38
NC_000005.9:g.139493801del , CM000667.1:g.139493801del GRCh37
NC_000005.8:g.139473985del NCBI36
NG_041813.1:g.5094del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.35del MANE Select ENSP00000332706.3:p.Gly12ValfsTer?
ENST00000505703.2:c.35del ENSP00000498560.1:p.Gly12ValfsTer?
ENST00000651386.1:c.35del ENSP00000499133.1:p.Gly12ValfsTer?
ENST00000331327.4:c.35del ENSP00000332706.3:p.Gly12ValfsTer?
ENST00000502351.1:n.458del
ENST00000505703.1:n.500del
NM_005859.4:c.35del NP_005850.1:p.Gly12ValfsTer?
NM_005859.5:c.35del MANE Select NP_005850.1:p.Gly12ValfsTer?