Canonical Allele Identifier: CA968819787
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1888624661
gnomAD v3: 15-38356500-TAAG-T
gnomAD v4: 15-38356500-TAAG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356502_38356504del , CM000677.2:g.38356502_38356504del GRCh38
NC_000015.9:g.38648703_38648705del , CM000677.1:g.38648703_38648705del GRCh37
NC_000015.8:g.36435995_36435997del NCBI36
NG_008980.1:g.108652_108654del

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4838_*4840del MANE Select ENSP00000299084.4:n.*4838_*4840del
ENST00000299084.8:c.*4838_*4840del ENSP00000299084.4:n.*4838_*4840del
NM_152594.2:c.*4838_*4840del NP_689807.1:n.*4838_*4840del
XM_005254202.3:c.*4838_*4840del XP_005254259.1:n.*4838_*4840del
XM_011521289.3:c.*4838_*4840del XP_011519591.1:n.*4838_*4840del
NM_152594.3:c.*4838_*4840del MANE Select NP_689807.1:n.*4838_*4840del
Search 100 bp 5'
Search 100 bp 3'