Canonical Allele Identifier: CA2675565244
Gene: PURA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114120del , CM000667.2:g.140114120del GRCh38
NC_000005.9:g.139493705del , CM000667.1:g.139493705del GRCh37
NC_000005.8:g.139473889del NCBI36
NG_041813.1:g.4998del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-62del MANE Select ENSP00000332706.3:n.-62del
ENST00000505703.2:c.-62del ENSP00000498560.1:n.-62del
ENST00000651386.1:c.-62del ENSP00000499133.1:n.-62del
ENST00000502351.1:n.362del
ENST00000505703.1:n.404del
NM_005859.5:c.-62del MANE Select NP_005850.1:n.-62del