Canonical Allele Identifier: CA7538025
Community Standard Title: NM_001363711.2(DUOX2):c.3061C>T (p.Arg1021Ter)
Gene: DUOX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45100173G>A , CM000677.2:g.45100173G>A GRCh38
NC_000015.9:g.45392371G>A , CM000677.1:g.45392371G>A GRCh37
NC_000015.8:g.43179663G>A NCBI36
NG_009447.1:g.18989C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001363711.2:c.3061C>T MANE Select NP_001350640.1:p.Arg1021Ter
ENST00000389039.11:c.3061C>T MANE Select ENSP00000373691.7:p.Arg1021Ter
NM_001363711.1:c.3061C>T NP_001350640.1:p.Arg1021Ter
NM_014080.4:c.3061C>T NP_054799.4:p.Arg1021Ter
NM_014080.5:c.3061C>T NP_054799.4:p.Arg1021Ter
ENST00000389039.10:c.3061C>T ENSP00000373691.6:p.Arg1021Ter
ENST00000558383.1:n.5676C>T
ENST00000560797.1:n.241C>T
ENST00000603300.1:c.3061C>T ENSP00000475084.1:p.Arg1021Ter
XM_005254421.2:c.3061C>T XP_005254478.1:p.Arg1021Ter