Canonical Allele Identifier: CA361490952
Gene: PURA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114699C>G , CM000667.2:g.140114699C>G GRCh38
NC_000005.9:g.139494284C>G , CM000667.1:g.139494284C>G GRCh37
NC_000005.8:g.139474468C>G NCBI36
NG_041813.1:g.5577C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.518C>G MANE Select ENSP00000332706.3:p.Thr173Arg
ENST00000651386.1:c.518C>G ENSP00000499133.1:p.Thr173Arg
ENST00000331327.4:c.518C>G ENSP00000332706.3:p.Thr173Arg
NM_005859.4:c.518C>G NP_005850.1:p.Thr173Arg
NM_005859.5:c.518C>G MANE Select NP_005850.1:p.Thr173Arg