Canonical Allele Identifier: CA446830737
Gene: PURA HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.139494489C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114904C>G , CM000667.2:g.140114904C>G GRCh38
NC_000005.9:g.139494489C>G , CM000667.1:g.139494489C>G GRCh37
NC_000005.8:g.139474673C>G NCBI36
NG_041813.1:g.5782C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.723C>G MANE Select ENSP00000332706.3:p.Gly241=
ENST00000651386.1:c.723C>G ENSP00000499133.1:p.Gly241=
ENST00000331327.4:c.723C>G ENSP00000332706.3:p.Gly241=
NM_005859.4:c.723C>G NP_005850.1:p.Gly241=
NM_005859.5:c.723C>G MANE Select NP_005850.1:p.Gly241=