Canonical Allele Identifier: CA7469958
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs757140393
ExAC: 15:38545459 CT / C
gnomAD v2: 15-38545459-CT-C
gnomAD v3: 15-38253258-CT-C
gnomAD v4: 15-38253258-CT-C
MyVariant Identifiers: chr15:g.38545460del (hg19) chr15:g.38253259del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253259del , CM000677.2:g.38253259del GRCh38
NC_000015.9:g.38545460del , CM000677.1:g.38545460del GRCh37
NC_000015.8:g.36332752del NCBI36
NG_008980.1:g.5409del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.32+42del MANE Select ENSP00000299084.4:n.32+42del
ENST00000299084.8:c.32+42del ENSP00000299084.4:n.32+42del
ENST00000561205.1:n.370+42del
ENST00000561317.1:c.-96+42del ENSP00000453680.1:n.-96+42del
NM_152594.2:c.32+42del NP_689807.1:n.32+42del
XM_005254202.2:c.32+42del XP_005254259.1:n.32+42del
XM_005254203.3:c.-16+42del XP_005254260.1:n.-16+42del
XM_005254202.3:c.32+42del XP_005254259.1:n.32+42del
XR_001751484.1:n.87+308del
NM_152594.3:c.32+42del MANE Select NP_689807.1:n.32+42del
Search 100 bp 5'
Search 100 bp 3'