Canonical Allele Identifier: CA1586594751
Gene: PURA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114665A= , CM000667.2:g.140114665A= GRCh38
NC_000005.9:g.139494250A= , CM000667.1:g.139494250A= GRCh37
NC_000005.8:g.139474434A= NCBI36
NG_041813.1:g.5543A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.484A= MANE Select ENSP00000332706.3:p.Asn162=
ENST00000651386.1:c.484A= ENSP00000499133.1:p.Asn162=
ENST00000331327.4:c.484A= ENSP00000332706.3:p.Asn162=
NM_005859.4:c.484A= NP_005850.1:p.Asn162=
NM_005859.5:c.484A= MANE Select NP_005850.1:p.Asn162=
Search 100 bp 5'
Search 100 bp 3'