Canonical Allele Identifier: CA1586595318
Gene: PURA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114786T= , CM000667.2:g.140114786T= GRCh38
NC_000005.9:g.139494371T= , CM000667.1:g.139494371T= GRCh37
NC_000005.8:g.139474555T= NCBI36
NG_041813.1:g.5664T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.605T= MANE Select ENSP00000332706.3:p.Leu202=
ENST00000651386.1:c.605T= ENSP00000499133.1:p.Leu202=
ENST00000331327.4:c.605T= ENSP00000332706.3:p.Leu202=
NM_005859.4:c.605T= NP_005850.1:p.Leu202=
NM_005859.5:c.605T= MANE Select NP_005850.1:p.Leu202=