Canonical Allele Identifier: CA2675565341
Gene: PURA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114157C>T , CM000667.2:g.140114157C>T GRCh38
NC_000005.9:g.139493742C>T , CM000667.1:g.139493742C>T GRCh37
NC_000005.8:g.139473926C>T NCBI36
NG_041813.1:g.5035C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-25C>T MANE Select ENSP00000332706.3:n.-25C>T
ENST00000505703.2:c.-25C>T ENSP00000498560.1:n.-25C>T
ENST00000651386.1:c.-25C>T ENSP00000499133.1:n.-25C>T
ENST00000331327.4:c.-25C>T ENSP00000332706.3:n.-25C>T
ENST00000502351.1:n.399C>T
ENST00000505703.1:n.441C>T
NM_005859.4:c.-25C>T NP_005850.1:n.-25C>T
NM_005859.5:c.-25C>T MANE Select NP_005850.1:n.-25C>T