Canonical Allele Identifier: CA1586592621
Gene: PURA HGNC NCBI

Linked Data

dbSNP Id: rs1763032747

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114135_140114137dup , CM000667.2:g.140114135_140114137dup GRCh38
NC_000005.9:g.139493720_139493722dup , CM000667.1:g.139493720_139493722dup GRCh37
NC_000005.8:g.139473904_139473906dup NCBI36
NG_041813.1:g.5013_5015dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-47_-45dup MANE Select ENSP00000332706.3:n.-47_-45dup
ENST00000505703.2:c.-47_-45dup ENSP00000498560.1:n.-47_-45dup
ENST00000651386.1:c.-47_-45dup ENSP00000499133.1:n.-47_-45dup
ENST00000331327.4:c.-47_-45dup ENSP00000332706.3:n.-47_-45dup
ENST00000502351.1:n.377_379dup
ENST00000505703.1:n.419_421dup
NM_005859.4:c.-47_-45dup NP_005850.1:n.-47_-45dup
NM_005859.5:c.-47_-45dup MANE Select NP_005850.1:n.-47_-45dup