Canonical Allele Identifier: CA347232899
Gene: SPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891518T>A , CM000664.2:g.72891518T>A GRCh38
NC_000002.11:g.73118647T>A , CM000664.1:g.73118647T>A GRCh37
NC_000002.10:g.72972155T>A NCBI36
NG_008234.1:g.9136T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.767T>A MANE Select ENSP00000234454.5:p.Val256Glu
ENST00000234454.5:c.767T>A ENSP00000234454.5:p.Val256Glu
ENST00000498749.1:n.712T>A
NM_003124.4:c.767T>A NP_003115.1:p.Val256Glu
NM_003124.5:c.767T>A MANE Select NP_003115.1:p.Val256Glu