Canonical Allele Identifier: CA1586593885
Gene: PURA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114443_140114446delinsATCG , CM000667.2:g.140114443_140114446delinsATCG GRCh38
NC_000005.9:g.139494028_139494031delinsATCG , CM000667.1:g.139494028_139494031delinsATCG GRCh37
NC_000005.8:g.139474212_139474215delinsATCG NCBI36
NG_041813.1:g.5321_5324delinsATCG

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.262_265delinsATCG MANE Select ENSP00000332706.3:p.Ile88=
ENST00000505703.2:c.262_265delinsATCG ENSP00000498560.1:p.Ile88=
ENST00000651386.1:c.262_265delinsATCG ENSP00000499133.1:p.Ile88=
ENST00000331327.4:c.262_265delinsATCG ENSP00000332706.3:p.Ile88=
NM_005859.4:c.262_265delinsATCG NP_005850.1:p.Ile88=
NM_005859.5:c.262_265delinsATCG MANE Select NP_005850.1:p.Ile88=
Search 100 bp 5'
Search 100 bp 3'