Canonical Allele Identifier: CA361490961
Gene: PURA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114705A>C , CM000667.2:g.140114705A>C GRCh38
NC_000005.9:g.139494290A>C , CM000667.1:g.139494290A>C GRCh37
NC_000005.8:g.139474474A>C NCBI36
NG_041813.1:g.5583A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.524A>C MANE Select ENSP00000332706.3:p.Asn175Thr
ENST00000651386.1:c.524A>C ENSP00000499133.1:p.Asn175Thr
ENST00000331327.4:c.524A>C ENSP00000332706.3:p.Asn175Thr
NM_005859.4:c.524A>C NP_005850.1:p.Asn175Thr
NM_005859.5:c.524A>C MANE Select NP_005850.1:p.Asn175Thr