Canonical Allele Identifier: CA1586593921
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114446G= , CM000667.2:g.140114446G= GRCh38
NC_000005.9:g.139494031G= , CM000667.1:g.139494031G= GRCh37
NC_000005.8:g.139474215G= NCBI36
NG_041813.1:g.5324G=

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.265G= MANE Select ENSP00000332706.3:p.Ala89=
ENST00000505703.2:c.265G= ENSP00000498560.1:p.Ala89=
ENST00000651386.1:c.265G= ENSP00000499133.1:p.Ala89=
ENST00000331327.4:c.265G= ENSP00000332706.3:p.Ala89=
NM_005859.4:c.265G= NP_005850.1:p.Ala89=
NM_005859.5:c.265G= MANE Select NP_005850.1:p.Ala89=