Canonical Allele Identifier: CA10635880
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 315730
ClinVar RCV Id: RCV000368494
dbSNP Id: rs886051102

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253034C>A , CM000677.2:g.38253034C>A GRCh38
NC_000015.9:g.38545235C>A , CM000677.1:g.38545235C>A GRCh37
NC_000015.8:g.36332527C>A NCBI36
NG_008980.1:g.5184C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-152C>A MANE Select ENSP00000299084.4:n.-152C>A
ENST00000299084.8:c.-152C>A ENSP00000299084.4:n.-152C>A
ENST00000561205.1:n.187C>A
NM_152594.2:c.-152C>A NP_689807.1:n.-152C>A
XM_005254202.2:c.-152C>A XP_005254259.1:n.-152C>A
XM_005254203.3:c.-199C>A XP_005254260.1:n.-199C>A
XM_005254202.3:c.-152C>A XP_005254259.1:n.-152C>A
XR_001751484.1:n.87+533G>T
NM_152594.3:c.-152C>A MANE Select NP_689807.1:n.-152C>A