Canonical Allele Identifier: CA1586592709
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1763033417
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114148A>C , CM000667.2:g.140114148A>C GRCh38
NC_000005.9:g.139493733A>C , CM000667.1:g.139493733A>C GRCh37
NC_000005.8:g.139473917A>C NCBI36
NG_041813.1:g.5026A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-34A>C MANE Select ENSP00000332706.3:n.-34A>C
ENST00000505703.2:c.-34A>C ENSP00000498560.1:n.-34A>C
ENST00000651386.1:c.-34A>C ENSP00000499133.1:n.-34A>C
ENST00000331327.4:c.-34A>C ENSP00000332706.3:n.-34A>C
ENST00000502351.1:n.390A>C
ENST00000505703.1:n.432A>C
NM_005859.4:c.-34A>C NP_005850.1:n.-34A>C
NM_005859.5:c.-34A>C MANE Select NP_005850.1:n.-34A>C
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