Canonical Allele Identifier: CA1586592532
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114109A= , CM000667.2:g.140114109A= GRCh38
NC_000005.9:g.139493694A= , CM000667.1:g.139493694A= GRCh37
NC_000005.8:g.139473878A= NCBI36
NG_041813.1:g.4987A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-73A= MANE Select ENSP00000332706.3:n.-73A=
ENST00000505703.2:c.-73A= ENSP00000498560.1:n.-73A=
ENST00000651386.1:c.-73A= ENSP00000499133.1:n.-73A=
ENST00000502351.1:n.351A=
ENST00000505703.1:n.393A=
NM_005859.5:c.-73A= MANE Select NP_005850.1:n.-73A=