Canonical Allele Identifier: CA269282659
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1978868
ClinVar RCV Id: RCV002765966 RCV003308262
dbSNP Id: rs779189071
gnomAD v2: 15-38545414-A-G
gnomAD v3: 15-38253213-A-G
gnomAD v4: 15-38253213-A-G
MyVariant Identifiers: chr15:g.38545414A>G (hg19) chr15:g.38253213A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253213A>G , CM000677.2:g.38253213A>G GRCh38
NC_000015.9:g.38545414A>G , CM000677.1:g.38545414A>G GRCh37
NC_000015.8:g.36332706A>G NCBI36
NG_008980.1:g.5363A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.28A>G MANE Select ENSP00000299084.4:p.Asn10Asp
ENST00000299084.8:c.28A>G ENSP00000299084.4:p.Asn10Asp
ENST00000561205.1:n.366A>G
ENST00000561317.1:c.-100A>G ENSP00000453680.1:n.-100A>G
NM_152594.2:c.28A>G NP_689807.1:p.Asn10Asp
XM_005254202.2:c.28A>G XP_005254259.1:p.Asn10Asp
XM_005254203.3:c.-20A>G XP_005254260.1:n.-20A>G
XM_005254202.3:c.28A>G XP_005254259.1:p.Asn10Asp
XR_001751484.1:n.87+354T>C
NM_152594.3:c.28A>G MANE Select NP_689807.1:p.Asn10Asp
Search 100 bp 5'
Search 100 bp 3'