Canonical Allele Identifier: CA361490543
Gene: PURA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114519A>C , CM000667.2:g.140114519A>C GRCh38
NC_000005.9:g.139494104A>C , CM000667.1:g.139494104A>C GRCh37
NC_000005.8:g.139474288A>C NCBI36
NG_041813.1:g.5397A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.338A>C MANE Select ENSP00000332706.3:p.Tyr113Ser
ENST00000651386.1:c.338A>C ENSP00000499133.1:p.Tyr113Ser
ENST00000331327.4:c.338A>C ENSP00000332706.3:p.Tyr113Ser
NM_005859.4:c.338A>C NP_005850.1:p.Tyr113Ser
NM_005859.5:c.338A>C MANE Select NP_005850.1:p.Tyr113Ser