Canonical Allele Identifier: CA1586595702
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114886G= , CM000667.2:g.140114886G= GRCh38
NC_000005.9:g.139494471G= , CM000667.1:g.139494471G= GRCh37
NC_000005.8:g.139474655G= NCBI36
NG_041813.1:g.5764G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.705G= MANE Select ENSP00000332706.3:p.Val235=
ENST00000651386.1:c.705G= ENSP00000499133.1:p.Val235=
ENST00000331327.4:c.705G= ENSP00000332706.3:p.Val235=
NM_005859.4:c.705G= NP_005850.1:p.Val235=
NM_005859.5:c.705G= MANE Select NP_005850.1:p.Val235=