Canonical Allele Identifier: CA1586592748
Gene: PURA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114162C= , CM000667.2:g.140114162C= GRCh38
NC_000005.9:g.139493747C= , CM000667.1:g.139493747C= GRCh37
NC_000005.8:g.139473931C= NCBI36
NG_041813.1:g.5040C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-20C= MANE Select ENSP00000332706.3:n.-20C=
ENST00000505703.2:c.-20C= ENSP00000498560.1:n.-20C=
ENST00000651386.1:c.-20C= ENSP00000499133.1:n.-20C=
ENST00000331327.4:c.-20C= ENSP00000332706.3:n.-20C=
ENST00000502351.1:n.404C=
ENST00000505703.1:n.446C=
NM_005859.4:c.-20C= NP_005850.1:n.-20C=
NM_005859.5:c.-20C= MANE Select NP_005850.1:n.-20C=
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