Canonical Allele Identifier: CA1260705250
Gene: SPR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891530A= , CM000664.2:g.72891530A= GRCh38
NC_000002.11:g.73118659A= , CM000664.1:g.73118659A= GRCh37
NC_000002.10:g.72972167A= NCBI36
NG_008234.1:g.9148A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.779A= MANE Select ENSP00000234454.5:p.Asp260=
ENST00000234454.5:c.779A= ENSP00000234454.5:p.Asp260=
ENST00000498749.1:n.724A=
NM_003124.4:c.779A= NP_003115.1:p.Asp260=
NM_003124.5:c.779A= MANE Select NP_003115.1:p.Asp260=
Search 100 bp 5'
Search 100 bp 3'