Canonical Allele Identifier: CA2675565331
Gene: PURA HGNC NCBI

Linked Data

gnomAD v4: 5-140114153-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114153G>T , CM000667.2:g.140114153G>T GRCh38
NC_000005.9:g.139493738G>T , CM000667.1:g.139493738G>T GRCh37
NC_000005.8:g.139473922G>T NCBI36
NG_041813.1:g.5031G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-29G>T MANE Select ENSP00000332706.3:n.-29G>T
ENST00000505703.2:c.-29G>T ENSP00000498560.1:n.-29G>T
ENST00000651386.1:c.-29G>T ENSP00000499133.1:n.-29G>T
ENST00000331327.4:c.-29G>T ENSP00000332706.3:n.-29G>T
ENST00000502351.1:n.395G>T
ENST00000505703.1:n.437G>T
NM_005859.4:c.-29G>T NP_005850.1:n.-29G>T
NM_005859.5:c.-29G>T MANE Select NP_005850.1:n.-29G>T
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