Canonical Allele Identifier: CA1260705322
Gene: SPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891705T= , CM000664.2:g.72891705T= GRCh38
NC_000002.11:g.73118834T= , CM000664.1:g.73118834T= GRCh37
NC_000002.10:g.72972342T= NCBI36
NG_008234.1:g.9323T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*168T= MANE Select ENSP00000234454.5:n.*168T=
ENST00000234454.5:c.*168T= ENSP00000234454.5:n.*168T=
ENST00000498749.1:n.899T=
NM_003124.4:c.*168T= NP_003115.1:n.*168T=
NM_003124.5:c.*168T= MANE Select NP_003115.1:n.*168T=