Canonical Allele Identifier: CA1586592291
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140113981T= , CM000667.2:g.140113981T= GRCh38
NC_000005.9:g.139493566T= , CM000667.1:g.139493566T= GRCh37
NC_000005.8:g.139473750T= NCBI36
NG_041813.1:g.4859T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505703.2:c.-141-60T= ENSP00000498560.1:n.-141-60T=
ENST00000651386.1:c.-141-60T= ENSP00000499133.1:n.-141-60T=
ENST00000502351.1:n.283-60T=
ENST00000505703.1:n.325-60T=