Canonical Allele Identifier: CA655953911
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253093del , CM000677.2:g.38253093del GRCh38
NC_000015.9:g.38545294del , CM000677.1:g.38545294del GRCh37
NC_000015.8:g.36332586del NCBI36
NG_008980.1:g.5243del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-93del MANE Select ENSP00000299084.4:n.-93del
ENST00000299084.8:c.-93del ENSP00000299084.4:n.-93del
ENST00000561205.1:n.246del
NM_152594.2:c.-93del NP_689807.1:n.-93del
XM_005254202.2:c.-93del XP_005254259.1:n.-93del
XM_005254203.3:c.-140del XP_005254260.1:n.-140del
XM_005254202.3:c.-93del XP_005254259.1:n.-93del
XR_001751484.1:n.87+480del
NM_152594.3:c.-93del MANE Select NP_689807.1:n.-93del