Canonical Allele Identifier: CA2695205323
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114452del , CM000667.2:g.140114452del GRCh38
NC_000005.9:g.139494037del , CM000667.1:g.139494037del GRCh37
NC_000005.8:g.139474221del NCBI36
NG_041813.1:g.5330del

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.271del MANE Select ENSP00000332706.3:p.Val91TrpfsTer?
ENST00000505703.2:c.271del ENSP00000498560.1:p.Val91TrpfsTer?
ENST00000651386.1:c.271del ENSP00000499133.1:p.Val91TrpfsTer?
ENST00000331327.4:c.271del ENSP00000332706.3:p.Val91TrpfsTer?
NM_005859.4:c.271del NP_005850.1:p.Val91TrpfsTer?
NM_005859.5:c.271del MANE Select NP_005850.1:p.Val91TrpfsTer?