Canonical Allele Identifier: CA1260705212
Gene: SPR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891418C= , CM000664.2:g.72891418C= GRCh38
NC_000002.11:g.73118547C= , CM000664.1:g.73118547C= GRCh37
NC_000002.10:g.72972055C= NCBI36
NG_008234.1:g.9036C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.667C= MANE Select ENSP00000234454.5:p.Gln223=
ENST00000234454.5:c.667C= ENSP00000234454.5:p.Gln223=
ENST00000498749.1:n.612C=
NM_003124.4:c.667C= NP_003115.1:p.Gln223=
NM_003124.5:c.667C= MANE Select NP_003115.1:p.Gln223=
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