Canonical Allele Identifier: CA1586595109
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114735G= , CM000667.2:g.140114735G= GRCh38
NC_000005.9:g.139494320G= , CM000667.1:g.139494320G= GRCh37
NC_000005.8:g.139474504G= NCBI36
NG_041813.1:g.5613G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.554G= MANE Select ENSP00000332706.3:p.Gly185=
ENST00000651386.1:c.554G= ENSP00000499133.1:p.Gly185=
ENST00000331327.4:c.554G= ENSP00000332706.3:p.Gly185=
NM_005859.4:c.554G= NP_005850.1:p.Gly185=
NM_005859.5:c.554G= MANE Select NP_005850.1:p.Gly185=