Canonical Allele Identifier: CA1586592322
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140113991G= , CM000667.2:g.140113991G= GRCh38
NC_000005.9:g.139493576G= , CM000667.1:g.139493576G= GRCh37
NC_000005.8:g.139473760G= NCBI36
NG_041813.1:g.4869G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505703.2:c.-141-50G= ENSP00000498560.1:n.-141-50G=
ENST00000651386.1:c.-141-50G= ENSP00000499133.1:n.-141-50G=
ENST00000502351.1:n.283-50G=
ENST00000505703.1:n.325-50G=