Canonical Allele Identifier: CA1586594681
Gene: PURA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114646C= , CM000667.2:g.140114646C= GRCh38
NC_000005.9:g.139494231C= , CM000667.1:g.139494231C= GRCh37
NC_000005.8:g.139474415C= NCBI36
NG_041813.1:g.5524C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.465C= MANE Select ENSP00000332706.3:p.Tyr155=
ENST00000651386.1:c.465C= ENSP00000499133.1:p.Tyr155=
ENST00000331327.4:c.465C= ENSP00000332706.3:p.Tyr155=
NM_005859.4:c.465C= NP_005850.1:p.Tyr155=
NM_005859.5:c.465C= MANE Select NP_005850.1:p.Tyr155=
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