Canonical Allele Identifier: CA2627714373
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253115del , CM000677.2:g.38253115del GRCh38
NC_000015.9:g.38545316del , CM000677.1:g.38545316del GRCh37
NC_000015.8:g.36332608del NCBI36
NG_008980.1:g.5265del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-71del MANE Select ENSP00000299084.4:n.-71del
ENST00000299084.8:c.-71del ENSP00000299084.4:n.-71del
ENST00000561205.1:n.268del
NM_152594.2:c.-71del NP_689807.1:n.-71del
XM_005254202.2:c.-71del XP_005254259.1:n.-71del
XM_005254203.3:c.-118del XP_005254260.1:n.-118del
XM_005254202.3:c.-71del XP_005254259.1:n.-71del
XR_001751484.1:n.87+455del
NM_152594.3:c.-71del MANE Select NP_689807.1:n.-71del