Canonical Allele Identifier: CA269282627
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs138385793
gnomAD v2: 15-38545143-T-A
gnomAD v3: 15-38252942-T-A
gnomAD v4: 15-38252942-T-A
MyVariant Identifiers: chr15:g.38545143T>A (hg19) chr15:g.38252942T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252942T>A , CM000677.2:g.38252942T>A GRCh38
NC_000015.9:g.38545143T>A , CM000677.1:g.38545143T>A GRCh37
NC_000015.8:g.36332435T>A NCBI36
NG_008980.1:g.5092T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-244T>A MANE Select ENSP00000299084.4:n.-244T>A
ENST00000299084.8:c.-244T>A ENSP00000299084.4:n.-244T>A
ENST00000561205.1:n.95T>A
NM_152594.2:c.-244T>A NP_689807.1:n.-244T>A
XM_005254202.2:c.-244T>A XP_005254259.1:n.-244T>A
XM_005254203.3:c.-291T>A XP_005254260.1:n.-291T>A
XM_005254202.3:c.-244T>A XP_005254259.1:n.-244T>A
XR_001751484.1:n.87+625A>T
NM_152594.3:c.-244T>A MANE Select NP_689807.1:n.-244T>A
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