Canonical Allele Identifier: CA1260705273
Gene: SPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891585T= , CM000664.2:g.72891585T= GRCh38
NC_000002.11:g.73118714T= , CM000664.1:g.73118714T= GRCh37
NC_000002.10:g.72972222T= NCBI36
NG_008234.1:g.9203T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*48T= MANE Select ENSP00000234454.5:n.*48T=
ENST00000234454.5:c.*48T= ENSP00000234454.5:n.*48T=
ENST00000498749.1:n.779T=
NM_003124.4:c.*48T= NP_003115.1:n.*48T=
NM_003124.5:c.*48T= MANE Select NP_003115.1:n.*48T=