Canonical Allele Identifier: CA361491392
Gene: PURA HGNC NCBI

Linked Data

ClinVar Variation Id: 959604
ClinVar RCV Id: RCV001232985 RCV002252338 RCV003232254
dbSNP Id: rs1763053854
MyVariant Identifiers: chr5:g.139494486C>G (hg19) chr5:g.140114901C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114901C>G , CM000667.2:g.140114901C>G GRCh38
NC_000005.9:g.139494486C>G , CM000667.1:g.139494486C>G GRCh37
NC_000005.8:g.139474670C>G NCBI36
NG_041813.1:g.5779C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.720C>G MANE Select ENSP00000332706.3:p.Tyr240Ter
ENST00000651386.1:c.720C>G ENSP00000499133.1:p.Tyr240Ter
ENST00000331327.4:c.720C>G ENSP00000332706.3:p.Tyr240Ter
NM_005859.4:c.720C>G NP_005850.1:p.Tyr240Ter
NM_005859.5:c.720C>G MANE Select NP_005850.1:p.Tyr240Ter
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