Canonical Allele Identifier: CA269282645
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs915882832
gnomAD v4: 15-38253086-G-GC
MyVariant Identifiers: chr15:g.38545287_38545288insC (hg19) chr15:g.38253086_38253087insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253093dup , CM000677.2:g.38253093dup GRCh38
NC_000015.9:g.38545294dup , CM000677.1:g.38545294dup GRCh37
NC_000015.8:g.36332586dup NCBI36
NG_008980.1:g.5243dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-93dup MANE Select ENSP00000299084.4:n.-93dup
ENST00000299084.8:c.-93dup ENSP00000299084.4:n.-93dup
ENST00000561205.1:n.246dup
NM_152594.2:c.-93dup NP_689807.1:n.-93dup
XM_005254202.2:c.-93dup XP_005254259.1:n.-93dup
XM_005254203.3:c.-140dup XP_005254260.1:n.-140dup
XM_005254202.3:c.-93dup XP_005254259.1:n.-93dup
XR_001751484.1:n.87+480dup
NM_152594.3:c.-93dup MANE Select NP_689807.1:n.-93dup
Search 100 bp 5'
Search 100 bp 3'