Canonical Allele Identifier: CA361490876
Gene: PURA HGNC NCBI

Linked Data

ClinVar Variation Id: 809808
ClinVar RCV Id: RCV000998446
dbSNP Id: rs1581036424
MyVariant Identifiers: chr5:g.139494250A>G (hg19) chr5:g.140114665A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114665A>G , CM000667.2:g.140114665A>G GRCh38
NC_000005.9:g.139494250A>G , CM000667.1:g.139494250A>G GRCh37
NC_000005.8:g.139474434A>G NCBI36
NG_041813.1:g.5543A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.484A>G MANE Select ENSP00000332706.3:p.Asn162Asp
ENST00000651386.1:c.484A>G ENSP00000499133.1:p.Asn162Asp
ENST00000331327.4:c.484A>G ENSP00000332706.3:p.Asn162Asp
NM_005859.4:c.484A>G NP_005850.1:p.Asn162Asp
NM_005859.5:c.484A>G MANE Select NP_005850.1:p.Asn162Asp
Search 100 bp 5'
Search 100 bp 3'