Canonical Allele Identifier: CA1586595831
Gene: PURA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114916A= , CM000667.2:g.140114916A= GRCh38
NC_000005.9:g.139494501A= , CM000667.1:g.139494501A= GRCh37
NC_000005.8:g.139474685A= NCBI36
NG_041813.1:g.5794A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.735A= MANE Select ENSP00000332706.3:p.Arg245=
ENST00000651386.1:c.735A= ENSP00000499133.1:p.Arg245=
ENST00000331327.4:c.735A= ENSP00000332706.3:p.Arg245=
NM_005859.4:c.735A= NP_005850.1:p.Arg245=
NM_005859.5:c.735A= MANE Select NP_005850.1:p.Arg245=
Search 100 bp 5'
Search 100 bp 3'