Canonical Allele Identifier: CA1586592726
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1763033644

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114156_140114167del , CM000667.2:g.140114156_140114167del GRCh38
NC_000005.9:g.139493741_139493752del , CM000667.1:g.139493741_139493752del GRCh37
NC_000005.8:g.139473925_139473936del NCBI36
NG_041813.1:g.5034_5045del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-26_-15del MANE Select ENSP00000332706.3:n.-26_-15del
ENST00000505703.2:c.-26_-15del ENSP00000498560.1:n.-26_-15del
ENST00000651386.1:c.-26_-15del ENSP00000499133.1:n.-26_-15del
ENST00000331327.4:c.-26_-15del ENSP00000332706.3:n.-26_-15del
ENST00000502351.1:n.398_409del
ENST00000505703.1:n.440_451del
NM_005859.4:c.-26_-15del NP_005850.1:n.-26_-15del
NM_005859.5:c.-26_-15del MANE Select NP_005850.1:n.-26_-15del