Canonical Allele Identifier: CA2575673125
Gene: SPRED1 HGNC NCBI

Linked Data

gnomAD v4: 15-38253275-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253280del , CM000677.2:g.38253280del GRCh38
NC_000015.9:g.38545481del , CM000677.1:g.38545481del GRCh37
NC_000015.8:g.36332773del NCBI36
NG_008980.1:g.5430del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.32+63del MANE Select ENSP00000299084.4:n.32+63del
ENST00000299084.8:c.32+63del ENSP00000299084.4:n.32+63del
ENST00000561205.1:n.370+63del
ENST00000561317.1:c.-96+63del ENSP00000453680.1:n.-96+63del
NM_152594.2:c.32+63del NP_689807.1:n.32+63del
XM_005254202.2:c.32+63del XP_005254259.1:n.32+63del
XM_005254203.3:c.-16+63del XP_005254260.1:n.-16+63del
XM_005254202.3:c.32+63del XP_005254259.1:n.32+63del
XR_001751484.1:n.87+291del
NM_152594.3:c.32+63del MANE Select NP_689807.1:n.32+63del
Search 100 bp 5'
Search 100 bp 3'