Canonical Allele Identifier: CA1586592598
Gene: PURA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114125A= , CM000667.2:g.140114125A= GRCh38
NC_000005.9:g.139493710A= , CM000667.1:g.139493710A= GRCh37
NC_000005.8:g.139473894A= NCBI36
NG_041813.1:g.5003A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-57A= MANE Select ENSP00000332706.3:n.-57A=
ENST00000505703.2:c.-57A= ENSP00000498560.1:n.-57A=
ENST00000651386.1:c.-57A= ENSP00000499133.1:n.-57A=
ENST00000331327.4:c.-57A= ENSP00000332706.3:n.-57A=
ENST00000502351.1:n.367A=
ENST00000505703.1:n.409A=
NM_005859.4:c.-57A= NP_005850.1:n.-57A=
NM_005859.5:c.-57A= MANE Select NP_005850.1:n.-57A=
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