Canonical Allele Identifier: CA2016939537

Gene: DUSP16

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12517293G= , CM000674.2:g.12517293G=	GRCh38
NC_000012.11:g.12670227G= , CM000674.1:g.12670227G=	GRCh37
NC_000012.10:g.12561494G=	NCBI36
NG_021402.1:g.50222C=
NG_021402.2:g.50222C=

Transcript Alleles

HGVS	Amino-acid Change
NM_030640.3:c.367+2569C= MANE Select	NP_085143.1:n.367+2569C=
ENST00000298573.9:c.367+2569C= MANE Select	ENSP00000298573.5:n.367+2569C=
NM_030640.2:c.367+2569C=	NP_085143.1:n.367+2569C=
ENST00000228862.3:c.367+2569C=	ENSP00000228862.3:n.367+2569C=
ENST00000298573.8:c.367+2569C=	ENSP00000298573.5:n.367+2569C=
XM_005253488.1:c.87+2569C=	XP_005253545.1:n.87+2569C=
XM_005253488.3:c.87+2569C=	XP_005253545.1:n.87+2569C=
XM_006719155.2:c.367+2569C=	XP_006719218.1:n.367+2569C=
XM_011520856.1:c.367+2569C=	XP_011519158.1:n.367+2569C=
XM_011520857.1:c.367+2569C=	XP_011519159.1:n.367+2569C=
XM_017019988.1:c.87+2569C=	XP_016875477.1:n.87+2569C=