Canonical Allele Identifier: CA1586592542
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114111_140114112delinsCG , CM000667.2:g.140114111_140114112delinsCG GRCh38
NC_000005.9:g.139493696_139493697delinsCG , CM000667.1:g.139493696_139493697delinsCG GRCh37
NC_000005.8:g.139473880_139473881delinsCG NCBI36
NG_041813.1:g.4989_4990delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-71_-70delinsCG MANE Select ENSP00000332706.3:n.-71_-70delinsCG
ENST00000505703.2:c.-71_-70delinsCG ENSP00000498560.1:n.-71_-70delinsCG
ENST00000651386.1:c.-71_-70delinsCG ENSP00000499133.1:n.-71_-70delinsCG
ENST00000502351.1:n.353_354delinsCG
ENST00000505703.1:n.395_396delinsCG
NM_005859.5:c.-71_-70delinsCG MANE Select NP_005850.1:n.-71_-70delinsCG