Canonical Allele Identifier: CA392276736

Gene: DUOX2

Linked Data

• MyVariant Identifiers: chr15:g.45400995C>T (hg19) ; chr15:g.45108797C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45108797C>T , CM000677.2:g.45108797C>T	GRCh38
NC_000015.9:g.45400995C>T , CM000677.1:g.45400995C>T	GRCh37
NC_000015.8:g.43188287C>T	NCBI36
NG_009447.1:g.10365G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389039.11:c.1390G>A MANE Select	ENSP00000373691.7:p.Asp464Asn
ENST00000389039.10:c.1390G>A	ENSP00000373691.6:p.Asp464Asn
ENST00000558383.1:n.2555G>A
ENST00000603300.1:c.1390G>A	ENSP00000475084.1:p.Asp464Asn
NM_014080.4:c.1390G>A	NP_054799.4:p.Asp464Asn
XM_005254421.2:c.1390G>A	XP_005254478.1:p.Asp464Asn
NM_001363711.1:c.1390G>A	NP_001350640.1:p.Asp464Asn
NM_001363711.2:c.1390G>A MANE Select	NP_001350640.1:p.Asp464Asn
NM_014080.5:c.1390G>A	NP_054799.4:p.Asp464Asn