Canonical Allele Identifier: CA645548775
Gene: PURA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114911dup , CM000667.2:g.140114911dup GRCh38
NC_000005.9:g.139494496dup , CM000667.1:g.139494496dup GRCh37
NC_000005.8:g.139474680dup NCBI36
NG_041813.1:g.5789dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.730dup MANE Select ENSP00000332706.3:p.Met244AsnfsTer?
ENST00000651386.1:c.730dup ENSP00000499133.1:p.Met244AsnfsTer?
ENST00000331327.4:c.730dup ENSP00000332706.3:p.Met244AsnfsTer?
NM_005859.4:c.730dup NP_005850.1:p.Met244AsnfsTer?
NM_005859.5:c.730dup MANE Select NP_005850.1:p.Met244AsnfsTer?