Canonical Allele Identifier: CA49798765
Gene: SPR HGNC NCBI

Linked Data

dbSNP Id: rs35103263
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891541dup , CM000664.2:g.72891541dup GRCh38
NC_000002.11:g.73118670dup , CM000664.1:g.73118670dup GRCh37
NC_000002.10:g.72972178dup NCBI36
NG_008234.1:g.9159dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*4dup MANE Select ENSP00000234454.5:n.*4dup
ENST00000234454.5:c.*4dup ENSP00000234454.5:n.*4dup
ENST00000498749.1:n.735dup
NM_003124.4:c.*4dup NP_003115.1:n.*4dup
NM_003124.5:c.*4dup MANE Select NP_003115.1:n.*4dup
Search 100 bp 5'
Search 100 bp 3'