Canonical Allele Identifier: CA2628241062
Gene: DUOX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45103894_45103903del , CM000677.2:g.45103894_45103903del GRCh38
NC_000015.9:g.45396092_45396101del , CM000677.1:g.45396092_45396101del GRCh37
NC_000015.8:g.43183384_43183393del NCBI36
NG_009447.1:g.15262_15271del

Transcript Alleles

HGVS Amino-acid change
ENST00000389039.11:c.2654+60_2654+69del MANE Select ENSP00000373691.7:n.2654+60_2654+69del
ENST00000389039.10:c.2654+60_2654+69del ENSP00000373691.6:n.2654+60_2654+69del
ENST00000558383.1:n.4385+60_4385+69del
ENST00000603300.1:c.2654+60_2654+69del ENSP00000475084.1:n.2654+60_2654+69del
NM_014080.4:c.2654+60_2654+69del NP_054799.4:n.2654+60_2654+69del
XM_005254421.2:c.2654+60_2654+69del XP_005254478.1:n.2654+60_2654+69del
NM_001363711.1:c.2654+60_2654+69del NP_001350640.1:n.2654+60_2654+69del
NM_001363711.2:c.2654+60_2654+69del MANE Select NP_001350640.1:n.2654+60_2654+69del
NM_014080.5:c.2654+60_2654+69del NP_054799.4:n.2654+60_2654+69del