Canonical Allele Identifier: CA1586595044
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114715T= , CM000667.2:g.140114715T= GRCh38
NC_000005.9:g.139494300T= , CM000667.1:g.139494300T= GRCh37
NC_000005.8:g.139474484T= NCBI36
NG_041813.1:g.5593T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.534T= MANE Select ENSP00000332706.3:p.Pro178=
ENST00000651386.1:c.534T= ENSP00000499133.1:p.Pro178=
ENST00000331327.4:c.534T= ENSP00000332706.3:p.Pro178=
NM_005859.4:c.534T= NP_005850.1:p.Pro178=
NM_005859.5:c.534T= MANE Select NP_005850.1:p.Pro178=