Canonical Allele Identifier: CA3437494
Gene: PURA HGNC NCBI

Linked Data

ClinVar Variation Id: 1129120
ClinVar RCV Id: RCV001462130
dbSNP Id: rs750557574
ExAC: 5:139494459 C / T
gnomAD v2: 5-139494459-C-T
gnomAD v3: 5-140114874-C-T
gnomAD v4: 5-140114874-C-T
MyVariant Identifiers: chr5:g.139494459C>T (hg19) chr5:g.140114874C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114874C>T , CM000667.2:g.140114874C>T GRCh38
NC_000005.9:g.139494459C>T , CM000667.1:g.139494459C>T GRCh37
NC_000005.8:g.139474643C>T NCBI36
NG_041813.1:g.5752C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.693C>T MANE Select ENSP00000332706.3:p.Phe231=
ENST00000651386.1:c.693C>T ENSP00000499133.1:p.Phe231=
ENST00000331327.4:c.693C>T ENSP00000332706.3:p.Phe231=
NM_005859.4:c.693C>T NP_005850.1:p.Phe231=
NM_005859.5:c.693C>T MANE Select NP_005850.1:p.Phe231=
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