Canonical Allele Identifier: CA1260705260
Gene: SPR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891546T= , CM000664.2:g.72891546T= GRCh38
NC_000002.11:g.73118675T= , CM000664.1:g.73118675T= GRCh37
NC_000002.10:g.72972183T= NCBI36
NG_008234.1:g.9164T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*9T= MANE Select ENSP00000234454.5:n.*9T=
ENST00000234454.5:c.*9T= ENSP00000234454.5:n.*9T=
ENST00000498749.1:n.740T=
NM_003124.4:c.*9T= NP_003115.1:n.*9T=
NM_003124.5:c.*9T= MANE Select NP_003115.1:n.*9T=
Search 100 bp 5'
Search 100 bp 3'