Canonical Allele Identifier: CA1586592566
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114114_140114115delinsCG , CM000667.2:g.140114114_140114115delinsCG GRCh38
NC_000005.9:g.139493699_139493700delinsCG , CM000667.1:g.139493699_139493700delinsCG GRCh37
NC_000005.8:g.139473883_139473884delinsCG NCBI36
NG_041813.1:g.4992_4993delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-68_-67delinsCG MANE Select ENSP00000332706.3:n.-68_-67delinsCG
ENST00000505703.2:c.-68_-67delinsCG ENSP00000498560.1:n.-68_-67delinsCG
ENST00000651386.1:c.-68_-67delinsCG ENSP00000499133.1:n.-68_-67delinsCG
ENST00000502351.1:n.356_357delinsCG
ENST00000505703.1:n.398_399delinsCG
NM_005859.5:c.-68_-67delinsCG MANE Select NP_005850.1:n.-68_-67delinsCG