Canonical Allele Identifier: CA1260705264
Gene: SPR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891562C= , CM000664.2:g.72891562C= GRCh38
NC_000002.11:g.73118691C= , CM000664.1:g.73118691C= GRCh37
NC_000002.10:g.72972199C= NCBI36
NG_008234.1:g.9180C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*25C= MANE Select ENSP00000234454.5:n.*25C=
ENST00000234454.5:c.*25C= ENSP00000234454.5:n.*25C=
ENST00000498749.1:n.756C=
NM_003124.4:c.*25C= NP_003115.1:n.*25C=
NM_003124.5:c.*25C= MANE Select NP_003115.1:n.*25C=
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