Canonical Allele Identifier: CA712588367
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1301332475
gnomAD v4: 15-38253149-C-A
MyVariant Identifiers: chr15:g.38545350C>A (hg19) chr15:g.38253149C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253149C>A , CM000677.2:g.38253149C>A GRCh38
NC_000015.9:g.38545350C>A , CM000677.1:g.38545350C>A GRCh37
NC_000015.8:g.36332642C>A NCBI36
NG_008980.1:g.5299C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-37C>A MANE Select ENSP00000299084.4:n.-37C>A
ENST00000299084.8:c.-37C>A ENSP00000299084.4:n.-37C>A
ENST00000561205.1:n.302C>A
NM_152594.2:c.-37C>A NP_689807.1:n.-37C>A
XM_005254202.2:c.-37C>A XP_005254259.1:n.-37C>A
XM_005254203.3:c.-84C>A XP_005254260.1:n.-84C>A
XM_005254202.3:c.-37C>A XP_005254259.1:n.-37C>A
XR_001751484.1:n.87+418G>T
NM_152594.3:c.-37C>A MANE Select NP_689807.1:n.-37C>A
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