Canonical Allele Identifier: CA7538035
Community Standard Title: NM_001363711.2(DUOX2):c.3033C>A (p.Tyr1011Ter)
Gene: DUOX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45100201G>T , CM000677.2:g.45100201G>T GRCh38
NC_000015.9:g.45392399G>T , CM000677.1:g.45392399G>T GRCh37
NC_000015.8:g.43179691G>T NCBI36
NG_009447.1:g.18961C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001363711.2:c.3033C>A MANE Select NP_001350640.1:p.Tyr1011Ter
ENST00000389039.11:c.3033C>A MANE Select ENSP00000373691.7:p.Tyr1011Ter
NM_001363711.1:c.3033C>A NP_001350640.1:p.Tyr1011Ter
NM_014080.4:c.3033C>A NP_054799.4:p.Tyr1011Ter
NM_014080.5:c.3033C>A NP_054799.4:p.Tyr1011Ter
ENST00000389039.10:c.3033C>A ENSP00000373691.6:p.Tyr1011Ter
ENST00000558383.1:n.5648C>A
ENST00000560797.1:n.213C>A
ENST00000603300.1:c.3033C>A ENSP00000475084.1:p.Tyr1011Ter
XM_005254421.2:c.3033C>A XP_005254478.1:p.Tyr1011Ter