Canonical Allele Identifier: CA2627714152
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252952del , CM000677.2:g.38252952del GRCh38
NC_000015.9:g.38545153del , CM000677.1:g.38545153del GRCh37
NC_000015.8:g.36332445del NCBI36
NG_008980.1:g.5102del

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-234del MANE Select ENSP00000299084.4:n.-234del
ENST00000299084.8:c.-234del ENSP00000299084.4:n.-234del
ENST00000561205.1:n.105del
NM_152594.2:c.-234del NP_689807.1:n.-234del
XM_005254202.2:c.-234del XP_005254259.1:n.-234del
XM_005254203.3:c.-281del XP_005254260.1:n.-281del
XM_005254202.3:c.-234del XP_005254259.1:n.-234del
XR_001751484.1:n.87+619del
NM_152594.3:c.-234del MANE Select NP_689807.1:n.-234del