Canonical Allele Identifier: CA490331441

Gene: DUOX2

Linked Data

• COSMIC: COSM5603436
• MyVariant Identifiers: chr15:g.45396169G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45103971G>A , CM000677.2:g.45103971G>A	GRCh38
NC_000015.9:g.45396169G>A , CM000677.1:g.45396169G>A	GRCh37
NC_000015.8:g.43183461G>A	NCBI36
NG_009447.1:g.15191C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389039.11:c.2643C>T MANE Select	ENSP00000373691.7:p.Phe881=
ENST00000389039.10:c.2643C>T	ENSP00000373691.6:p.Phe881=
ENST00000558383.1:n.4374C>T
ENST00000603300.1:c.2643C>T	ENSP00000475084.1:p.Phe881=
NM_014080.4:c.2643C>T	NP_054799.4:p.Phe881=
XM_005254421.2:c.2643C>T	XP_005254478.1:p.Phe881=
NM_001363711.1:c.2643C>T	NP_001350640.1:p.Phe881=
NM_001363711.2:c.2643C>T MANE Select	NP_001350640.1:p.Phe881=
NM_014080.5:c.2643C>T	NP_054799.4:p.Phe881=