Canonical Allele Identifier: CA1586593895
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114444_140114445delinsTC , CM000667.2:g.140114444_140114445delinsTC GRCh38
NC_000005.9:g.139494029_139494030delinsTC , CM000667.1:g.139494029_139494030delinsTC GRCh37
NC_000005.8:g.139474213_139474214delinsTC NCBI36
NG_041813.1:g.5322_5323delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.263_264delinsTC MANE Select ENSP00000332706.3:p.Ile88=
ENST00000505703.2:c.263_264delinsTC ENSP00000498560.1:p.Ile88=
ENST00000651386.1:c.263_264delinsTC ENSP00000499133.1:p.Ile88=
ENST00000331327.4:c.263_264delinsTC ENSP00000332706.3:p.Ile88=
NM_005859.4:c.263_264delinsTC NP_005850.1:p.Ile88=
NM_005859.5:c.263_264delinsTC MANE Select NP_005850.1:p.Ile88=