Canonical Allele Identifier: CA392276737
Gene: DUOX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45108799A>C , CM000677.2:g.45108799A>C GRCh38
NC_000015.9:g.45400997A>C , CM000677.1:g.45400997A>C GRCh37
NC_000015.8:g.43188289A>C NCBI36
NG_009447.1:g.10363T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389039.11:c.1388T>G MANE Select ENSP00000373691.7:p.Val463Gly
ENST00000389039.10:c.1388T>G ENSP00000373691.6:p.Val463Gly
ENST00000558383.1:n.2553T>G
ENST00000603300.1:c.1388T>G ENSP00000475084.1:p.Val463Gly
NM_014080.4:c.1388T>G NP_054799.4:p.Val463Gly
XM_005254421.2:c.1388T>G XP_005254478.1:p.Val463Gly
NM_001363711.1:c.1388T>G NP_001350640.1:p.Val463Gly
NM_001363711.2:c.1388T>G MANE Select NP_001350640.1:p.Val463Gly
NM_014080.5:c.1388T>G NP_054799.4:p.Val463Gly