Canonical Allele Identifier: CA1586595865
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114930A= , CM000667.2:g.140114930A= GRCh38
NC_000005.9:g.139494515A= , CM000667.1:g.139494515A= GRCh37
NC_000005.8:g.139474699A= NCBI36
NG_041813.1:g.5808A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.749A= MANE Select ENSP00000332706.3:p.Lys250=
ENST00000651386.1:c.749A= ENSP00000499133.1:p.Lys250=
ENST00000331327.4:c.749A= ENSP00000332706.3:p.Lys250=
NM_005859.4:c.749A= NP_005850.1:p.Lys250=
NM_005859.5:c.749A= MANE Select NP_005850.1:p.Lys250=