Canonical Allele Identifier: CA1257217361
Gene: SPRED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381815_65381816delinsAC , CM000664.2:g.65381815_65381816delinsAC GRCh38
NC_000002.11:g.65608949_65608950delinsAC , CM000664.1:g.65608949_65608950delinsAC GRCh37
NC_000002.10:g.65462453_65462454delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356388.9:c.27-36920_27-36919delinsGT MANE Select ENSP00000348753.4:n.27-36920_27-36919deli...
ENST00000356388.8:c.27-36920_27-36919delinsGT ENSP00000348753.4:n.27-36920_27-36919deli...
ENST00000440972.1:c.27-36920_27-36919delinsGT ENSP00000406481.1:n.27-36920_27-36919deli...
NM_181784.2:c.27-36920_27-36919delinsGT NP_861449.2:n.27-36920_27-36919delinsGT
XM_005264200.3:c.27-36920_27-36919delinsGT XP_005264257.2:n.27-36920_27-36919delinsG...
XM_005264202.3:c.27-36920_27-36919delinsGT XP_005264259.1:n.27-36920_27-36919delinsG...
XM_006711966.1:c.27-36920_27-36919delinsGT XP_006712029.1:n.27-36920_27-36919delinsG...
XM_005264200.5:c.27-36920_27-36919delinsGT XP_005264257.2:n.27-36920_27-36919delinsG...
XM_005264202.5:c.27-36920_27-36919delinsGT XP_005264259.1:n.27-36920_27-36919delinsG...
NM_181784.3:c.27-36920_27-36919delinsGT MANE Select NP_861449.2:n.27-36920_27-36919delinsGT