Canonical Allele Identifier: CA617495176
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1200742582

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253159_38253160insGGAGATCA , CM000677.2:g.38253159_38253160insGGAGATCA GRCh38
NC_000015.9:g.38545360_38545361insGGAGATCA , CM000677.1:g.38545360_38545361insGGAGATCA GRCh37
NC_000015.8:g.36332652_36332653insGGAGATCA NCBI36
NG_008980.1:g.5309_5310insGGAGATCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-27_-26insGGAGATCA MANE Select ENSP00000299084.4:n.-27_-26insGGAGATCA
ENST00000299084.8:c.-27_-26insGGAGATCA ENSP00000299084.4:n.-27_-26insGGAGATCA
ENST00000561205.1:n.312_313insGGAGATCA
NM_152594.2:c.-27_-26insGGAGATCA NP_689807.1:n.-27_-26insGGAGATCA
XM_005254202.2:c.-27_-26insGGAGATCA XP_005254259.1:n.-27_-26insGGAGATCA
XM_005254203.3:c.-74_-73insGGAGATCA XP_005254260.1:n.-74_-73insGGAGATCA
XM_005254202.3:c.-27_-26insGGAGATCA XP_005254259.1:n.-27_-26insGGAGATCA
XR_001751484.1:n.87+407_87+408insTGATCTCC
NM_152594.3:c.-27_-26insGGAGATCA MANE Select NP_689807.1:n.-27_-26insGGAGATCA