Canonical Allele Identifier: CA2627714505
Gene: SPRED1 HGNC NCBI

Linked Data

gnomAD v4: 15-38253269-CG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253271del , CM000677.2:g.38253271del GRCh38
NC_000015.9:g.38545472del , CM000677.1:g.38545472del GRCh37
NC_000015.8:g.36332764del NCBI36
NG_008980.1:g.5421del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.32+54del MANE Select ENSP00000299084.4:n.32+54del
ENST00000299084.8:c.32+54del ENSP00000299084.4:n.32+54del
ENST00000561205.1:n.370+54del
ENST00000561317.1:c.-96+54del ENSP00000453680.1:n.-96+54del
NM_152594.2:c.32+54del NP_689807.1:n.32+54del
XM_005254202.2:c.32+54del XP_005254259.1:n.32+54del
XM_005254203.3:c.-16+54del XP_005254260.1:n.-16+54del
XM_005254202.3:c.32+54del XP_005254259.1:n.32+54del
XR_001751484.1:n.87+297del
NM_152594.3:c.32+54del MANE Select NP_689807.1:n.32+54del
Search 100 bp 5'
Search 100 bp 3'