Canonical Allele Identifier: CA392268438
Gene: DUOX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45103963A>T , CM000677.2:g.45103963A>T GRCh38
NC_000015.9:g.45396161A>T , CM000677.1:g.45396161A>T GRCh37
NC_000015.8:g.43183453A>T NCBI36
NG_009447.1:g.15199T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389039.11:c.2651T>A MANE Select ENSP00000373691.7:p.Met884Lys
ENST00000389039.10:c.2651T>A ENSP00000373691.6:p.Met884Lys
ENST00000558383.1:n.4382T>A
ENST00000603300.1:c.2651T>A ENSP00000475084.1:p.Met884Lys
NM_014080.4:c.2651T>A NP_054799.4:p.Met884Lys
XM_005254421.2:c.2651T>A XP_005254478.1:p.Met884Lys
NM_001363711.1:c.2651T>A NP_001350640.1:p.Met884Lys
NM_001363711.2:c.2651T>A MANE Select NP_001350640.1:p.Met884Lys
NM_014080.5:c.2651T>A NP_054799.4:p.Met884Lys