Canonical Allele Identifier: CA1586595265
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114776C= , CM000667.2:g.140114776C= GRCh38
NC_000005.9:g.139494361C= , CM000667.1:g.139494361C= GRCh37
NC_000005.8:g.139474545C= NCBI36
NG_041813.1:g.5654C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.595C= MANE Select ENSP00000332706.3:p.Arg199=
ENST00000651386.1:c.595C= ENSP00000499133.1:p.Arg199=
ENST00000331327.4:c.595C= ENSP00000332706.3:p.Arg199=
NM_005859.4:c.595C= NP_005850.1:p.Arg199=
NM_005859.5:c.595C= MANE Select NP_005850.1:p.Arg199=