Canonical Allele Identifier: CA392276744
Gene: DUOX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45108802T>A , CM000677.2:g.45108802T>A GRCh38
NC_000015.9:g.45401000T>A , CM000677.1:g.45401000T>A GRCh37
NC_000015.8:g.43188292T>A NCBI36
NG_009447.1:g.10360A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389039.11:c.1385A>T MANE Select ENSP00000373691.7:p.Asn462Ile
ENST00000389039.10:c.1385A>T ENSP00000373691.6:p.Asn462Ile
ENST00000558383.1:n.2550A>T
ENST00000603300.1:c.1385A>T ENSP00000475084.1:p.Asn462Ile
NM_014080.4:c.1385A>T NP_054799.4:p.Asn462Ile
XM_005254421.2:c.1385A>T XP_005254478.1:p.Asn462Ile
NM_001363711.1:c.1385A>T NP_001350640.1:p.Asn462Ile
NM_001363711.2:c.1385A>T MANE Select NP_001350640.1:p.Asn462Ile
NM_014080.5:c.1385A>T NP_054799.4:p.Asn462Ile