Canonical Allele Identifier: CA2573052438
Gene: PURA HGNC NCBI

Linked Data

ClinVar Variation Id: 1334710
ClinVar RCV Id: RCV001814891
dbSNP Id: rs2126749210

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114711_140114712dup , CM000667.2:g.140114711_140114712dup GRCh38
NC_000005.9:g.139494296_139494297dup , CM000667.1:g.139494296_139494297dup GRCh37
NC_000005.8:g.139474480_139474481dup NCBI36
NG_041813.1:g.5589_5590dup

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.530_531dup MANE Select ENSP00000332706.3:p.Pro178GlyfsTer?
ENST00000651386.1:c.530_531dup ENSP00000499133.1:p.Pro178GlyfsTer?
ENST00000331327.4:c.530_531dup ENSP00000332706.3:p.Pro178GlyfsTer?
NM_005859.4:c.530_531dup NP_005850.1:p.Pro178GlyfsTer?
NM_005859.5:c.530_531dup MANE Select NP_005850.1:p.Pro178GlyfsTer?