Canonical Allele Identifier: CA2173935198
Gene: DUOX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45108870G= , CM000677.2:g.45108870G= GRCh38
NC_000015.9:g.45401068G= , CM000677.1:g.45401068G= GRCh37
NC_000015.8:g.43188360G= NCBI36
NG_009447.1:g.10292C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389039.11:c.1317C= MANE Select ENSP00000373691.7:p.Pro439=
ENST00000389039.10:c.1317C= ENSP00000373691.6:p.Pro439=
ENST00000558383.1:n.2482C=
ENST00000603300.1:c.1317C= ENSP00000475084.1:p.Pro439=
NM_014080.4:c.1317C= NP_054799.4:p.Pro439=
XM_005254421.2:c.1317C= XP_005254478.1:p.Pro439=
NM_001363711.1:c.1317C= NP_001350640.1:p.Pro439=
NM_001363711.2:c.1317C= MANE Select NP_001350640.1:p.Pro439=
NM_014080.5:c.1317C= NP_054799.4:p.Pro439=