Canonical Allele Identifier: CA392276747

Gene: DUOX2

Linked Data

• MyVariant Identifiers: chr15:g.45401001T>A (hg19) ; chr15:g.45108803T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45108803T>A , CM000677.2:g.45108803T>A	GRCh38
NC_000015.9:g.45401001T>A , CM000677.1:g.45401001T>A	GRCh37
NC_000015.8:g.43188293T>A	NCBI36
NG_009447.1:g.10359A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389039.11:c.1384A>T MANE Select	ENSP00000373691.7:p.Asn462Tyr
ENST00000389039.10:c.1384A>T	ENSP00000373691.6:p.Asn462Tyr
ENST00000558383.1:n.2549A>T
ENST00000603300.1:c.1384A>T	ENSP00000475084.1:p.Asn462Tyr
NM_014080.4:c.1384A>T	NP_054799.4:p.Asn462Tyr
XM_005254421.2:c.1384A>T	XP_005254478.1:p.Asn462Tyr
NM_001363711.1:c.1384A>T	NP_001350640.1:p.Asn462Tyr
NM_001363711.2:c.1384A>T MANE Select	NP_001350640.1:p.Asn462Tyr
NM_014080.5:c.1384A>T	NP_054799.4:p.Asn462Tyr