Canonical Allele Identifier: CA347232927
Gene: SPR HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.779A>C MANE Select ENSP00000234454.5:p.Asp260Ala
ENST00000234454.5:c.779A>C ENSP00000234454.5:p.Asp260Ala
ENST00000498749.1:n.724A>C
NM_003124.4:c.779A>C NP_003115.1:p.Asp260Ala
NM_003124.5:c.779A>C MANE Select NP_003115.1:p.Asp260Ala