Canonical Allele Identifier: CA1586594076
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114483C= , CM000667.2:g.140114483C= GRCh38
NC_000005.9:g.139494068C= , CM000667.1:g.139494068C= GRCh37
NC_000005.8:g.139474252C= NCBI36
NG_041813.1:g.5361C=

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.302C= MANE Select ENSP00000332706.3:p.Thr101=
ENST00000505703.2:c.302C= ENSP00000498560.1:p.Thr101=
ENST00000651386.1:c.302C= ENSP00000499133.1:p.Thr101=
ENST00000331327.4:c.302C= ENSP00000332706.3:p.Thr101=
NM_005859.4:c.302C= NP_005850.1:p.Thr101=
NM_005859.5:c.302C= MANE Select NP_005850.1:p.Thr101=