Canonical Allele Identifier: CA2768634940
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114148del , CM000667.2:g.140114148del GRCh38
NC_000005.9:g.139493733del , CM000667.1:g.139493733del GRCh37
NC_000005.8:g.139473917del NCBI36
NG_041813.1:g.5026del

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-34del MANE Select ENSP00000332706.3:n.-34del
ENST00000505703.2:c.-34del ENSP00000498560.1:n.-34del
ENST00000651386.1:c.-34del ENSP00000499133.1:n.-34del
ENST00000331327.4:c.-34del ENSP00000332706.3:n.-34del
ENST00000502351.1:n.390del
ENST00000505703.1:n.432del
NM_005859.4:c.-34del NP_005850.1:n.-34del
NM_005859.5:c.-34del MANE Select NP_005850.1:n.-34del