Canonical Allele Identifier: CA10635884
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 315731
dbSNP Id: rs192699510

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-93C>T MANE Select ENSP00000299084.4:n.-93C>T
ENST00000299084.8:c.-93C>T ENSP00000299084.4:n.-93C>T
ENST00000561205.1:n.246C>T
NM_152594.2:c.-93C>T NP_689807.1:n.-93C>T
XM_005254202.2:c.-93C>T XP_005254259.1:n.-93C>T
XM_005254203.3:c.-140C>T XP_005254260.1:n.-140C>T
XM_005254202.3:c.-93C>T XP_005254259.1:n.-93C>T
XR_001751484.1:n.87+474G>A
NM_152594.3:c.-93C>T MANE Select NP_689807.1:n.-93C>T