Canonical Allele Identifier: CA2675565289
Gene: PURA HGNC NCBI

Linked Data

gnomAD v4: 5-140114139-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114139C>A , CM000667.2:g.140114139C>A GRCh38
NC_000005.9:g.139493724C>A , CM000667.1:g.139493724C>A GRCh37
NC_000005.8:g.139473908C>A NCBI36
NG_041813.1:g.5017C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-43C>A MANE Select ENSP00000332706.3:n.-43C>A
ENST00000505703.2:c.-43C>A ENSP00000498560.1:n.-43C>A
ENST00000651386.1:c.-43C>A ENSP00000499133.1:n.-43C>A
ENST00000331327.4:c.-43C>A ENSP00000332706.3:n.-43C>A
ENST00000502351.1:n.381C>A
ENST00000505703.1:n.423C>A
NM_005859.4:c.-43C>A NP_005850.1:n.-43C>A
NM_005859.5:c.-43C>A MANE Select NP_005850.1:n.-43C>A
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