Canonical Allele Identifier: CA2675565317
Gene: PURA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114156_140114161del , CM000667.2:g.140114156_140114161del GRCh38
NC_000005.9:g.139493741_139493746del , CM000667.1:g.139493741_139493746del GRCh37
NC_000005.8:g.139473925_139473930del NCBI36
NG_041813.1:g.5034_5039del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-26_-21del MANE Select ENSP00000332706.3:n.-26_-21del
ENST00000505703.2:c.-26_-21del ENSP00000498560.1:n.-26_-21del
ENST00000651386.1:c.-26_-21del ENSP00000499133.1:n.-26_-21del
ENST00000331327.4:c.-26_-21del ENSP00000332706.3:n.-26_-21del
ENST00000502351.1:n.398_403del
ENST00000505703.1:n.440_445del
NM_005859.4:c.-26_-21del NP_005850.1:n.-26_-21del
NM_005859.5:c.-26_-21del MANE Select NP_005850.1:n.-26_-21del