Canonical Allele Identifier: CA1586592721
Gene: PURA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114152G= , CM000667.2:g.140114152G= GRCh38
NC_000005.9:g.139493737G= , CM000667.1:g.139493737G= GRCh37
NC_000005.8:g.139473921G= NCBI36
NG_041813.1:g.5030G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-30G= MANE Select ENSP00000332706.3:n.-30G=
ENST00000505703.2:c.-30G= ENSP00000498560.1:n.-30G=
ENST00000651386.1:c.-30G= ENSP00000499133.1:n.-30G=
ENST00000331327.4:c.-30G= ENSP00000332706.3:n.-30G=
ENST00000502351.1:n.394G=
ENST00000505703.1:n.436G=
NM_005859.4:c.-30G= NP_005850.1:n.-30G=
NM_005859.5:c.-30G= MANE Select NP_005850.1:n.-30G=
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