Canonical Allele Identifier: CA7538011
Community Standard Title: NM_001363711.2(DUOX2):c.3103G>A (p.Val1035Met)
Gene: DUOX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45100131C>T , CM000677.2:g.45100131C>T GRCh38
NC_000015.9:g.45392329C>T , CM000677.1:g.45392329C>T GRCh37
NC_000015.8:g.43179621C>T NCBI36
NG_009447.1:g.19031G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001363711.2:c.3103G>A MANE Select NP_001350640.1:p.Val1035Met
ENST00000389039.11:c.3103G>A MANE Select ENSP00000373691.7:p.Val1035Met
NM_001363711.1:c.3103G>A NP_001350640.1:p.Val1035Met
NM_014080.4:c.3103G>A NP_054799.4:p.Val1035Met
NM_014080.5:c.3103G>A NP_054799.4:p.Val1035Met
ENST00000389039.10:c.3103G>A ENSP00000373691.6:p.Val1035Met
ENST00000558383.1:n.5718G>A
ENST00000560797.1:n.283G>A
ENST00000603300.1:c.3103G>A ENSP00000475084.1:p.Val1035Met
XM_005254421.2:c.3103G>A XP_005254478.1:p.Val1035Met