Canonical Allele Identifier: CA2170814973
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356500_38356503delinsTAAG , CM000677.2:g.38356500_38356503delinsTAAG GRCh38
NC_000015.9:g.38648701_38648704delinsTAAG , CM000677.1:g.38648701_38648704delinsTAAG GRCh37
NC_000015.8:g.36435993_36435996delinsTAAG NCBI36
NG_008980.1:g.108650_108653delinsTAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4836_*4839delinsTAAG MANE Select ENSP00000299084.4:n.*4836_*4839delinsTAAG...
ENST00000299084.8:c.*4836_*4839delinsTAAG ENSP00000299084.4:n.*4836_*4839delinsTAAG...
NM_152594.2:c.*4836_*4839delinsTAAG NP_689807.1:n.*4836_*4839delinsTAAG
XM_005254202.3:c.*4836_*4839delinsTAAG XP_005254259.1:n.*4836_*4839delinsTAAG
XM_011521289.3:c.*4836_*4839delinsTAAG XP_011519591.1:n.*4836_*4839delinsTAAG
NM_152594.3:c.*4836_*4839delinsTAAG MANE Select NP_689807.1:n.*4836_*4839delinsTAAG