Canonical Allele Identifier: CA1260705291
Gene: SPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891625G= , CM000664.2:g.72891625G= GRCh38
NC_000002.11:g.73118754G= , CM000664.1:g.73118754G= GRCh37
NC_000002.10:g.72972262G= NCBI36
NG_008234.1:g.9243G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*88G= MANE Select ENSP00000234454.5:n.*88G=
ENST00000234454.5:c.*88G= ENSP00000234454.5:n.*88G=
ENST00000498749.1:n.819G=
NM_003124.4:c.*88G= NP_003115.1:n.*88G=
NM_003124.5:c.*88G= MANE Select NP_003115.1:n.*88G=