Canonical Allele Identifier: CA658761219
Gene: SPRED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253207del , CM000677.2:g.38253207del GRCh38
NC_000015.9:g.38545408del , CM000677.1:g.38545408del GRCh37
NC_000015.8:g.36332700del NCBI36
NG_008980.1:g.5357del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.22del MANE Select ENSP00000299084.4:p.Ser8LeufsTer14
ENST00000299084.8:c.22del ENSP00000299084.4:p.Ser8LeufsTer14
ENST00000561205.1:n.360del
ENST00000561317.1:c.-106del ENSP00000453680.1:n.-106del
NM_152594.2:c.22del NP_689807.1:p.Ser8LeufsTer14
XM_005254202.2:c.22del XP_005254259.1:p.Ser8LeufsTer26
XM_005254203.3:c.-26del XP_005254260.1:n.-26del
XM_005254202.3:c.22del XP_005254259.1:p.Ser8LeufsTer26
XR_001751484.1:n.87+361del
NM_152594.3:c.22del MANE Select NP_689807.1:p.Ser8LeufsTer14
Search 100 bp 5'
Search 100 bp 3'