Canonical Allele Identifier: CA446831158
Gene: PURA HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.139494426G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114841G>A , CM000667.2:g.140114841G>A GRCh38
NC_000005.9:g.139494426G>A , CM000667.1:g.139494426G>A GRCh37
NC_000005.8:g.139474610G>A NCBI36
NG_041813.1:g.5719G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.660G>A MANE Select ENSP00000332706.3:p.Glu220=
ENST00000651386.1:c.660G>A ENSP00000499133.1:p.Glu220=
ENST00000331327.4:c.660G>A ENSP00000332706.3:p.Glu220=
NM_005859.4:c.660G>A NP_005850.1:p.Glu220=
NM_005859.5:c.660G>A MANE Select NP_005850.1:p.Glu220=