Canonical Allele Identifier: CA446830739
Gene: PURA HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.139494492G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114907G>T , CM000667.2:g.140114907G>T GRCh38
NC_000005.9:g.139494492G>T , CM000667.1:g.139494492G>T GRCh37
NC_000005.8:g.139474676G>T NCBI36
NG_041813.1:g.5785G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.726G>T MANE Select ENSP00000332706.3:p.Val242=
ENST00000651386.1:c.726G>T ENSP00000499133.1:p.Val242=
ENST00000331327.4:c.726G>T ENSP00000332706.3:p.Val242=
NM_005859.4:c.726G>T NP_005850.1:p.Val242=
NM_005859.5:c.726G>T MANE Select NP_005850.1:p.Val242=