Canonical Allele Identifier: CA2627714207
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252995_38252997del , CM000677.2:g.38252995_38252997del GRCh38
NC_000015.9:g.38545196_38545198del , CM000677.1:g.38545196_38545198del GRCh37
NC_000015.8:g.36332488_36332490del NCBI36
NG_008980.1:g.5145_5147del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-191_-189del MANE Select ENSP00000299084.4:n.-191_-189del
ENST00000299084.8:c.-191_-189del ENSP00000299084.4:n.-191_-189del
ENST00000561205.1:n.148_150del
NM_152594.2:c.-191_-189del NP_689807.1:n.-191_-189del
XM_005254202.2:c.-191_-189del XP_005254259.1:n.-191_-189del
XM_005254203.3:c.-238_-236del XP_005254260.1:n.-238_-236del
XM_005254202.3:c.-191_-189del XP_005254259.1:n.-191_-189del
XR_001751484.1:n.87+573_87+575del
NM_152594.3:c.-191_-189del MANE Select NP_689807.1:n.-191_-189del