Canonical Allele Identifier: CA2564378385

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914730_12914731del , CM000686.2:g.12914730_12914731del	GRCh38
NC_000024.9:g.15026642_15026643del , CM000686.1:g.15026642_15026643del	GRCh37
NC_000024.8:g.13536036_13536037del	NCBI36
NG_012831.1:g.15624_15625del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.759+81_759+82del MANE Select	ENSP00000336725.3:n.759+81_759+82del
ENST00000336079.7:c.759+81_759+82del	ENSP00000336725.3:n.759+81_759+82del
ENST00000360160.8:c.759+81_759+82del	ENSP00000353284.4:n.759+81_759+82del
ENST00000463199.1:n.277+81_277+82del
ENST00000472510.5:n.403_404del
NM_001122665.2:c.759+81_759+82del	NP_001116137.1:n.759+81_759+82del
NM_001302552.1:c.750+81_750+82del	NP_001289481.1:n.750+81_750+82del
NM_004660.4:c.759+81_759+82del	NP_004651.2:n.759+81_759+82del
XM_006724878.1:c.759+81_759+82del	XP_006724941.1:n.759+81_759+82del
XM_011531471.1:c.759+81_759+82del	XP_011529773.1:n.759+81_759+82del
NM_001122665.3:c.759+81_759+82del	NP_001116137.1:n.759+81_759+82del
NM_001302552.2:c.750+81_750+82del	NP_001289481.1:n.750+81_750+82del
NM_001324195.1:c.759+81_759+82del	NP_001311124.1:n.759+81_759+82del
NR_136716.1:n.991_992del
NR_136717.1:n.990+81_990+82del
NR_136718.1:n.1071_1072del
NR_136719.1:n.861_862del
NR_136720.1:n.991_992del
NR_136721.1:n.838+81_838+82del
NR_136722.1:n.905+81_905+82del
NR_136723.1:n.986_987del
NR_136724.1:n.906_907del
XR_001756014.2:n.863+81_863+82del
NM_004660.5:c.759+81_759+82del MANE Select	NP_004651.2:n.759+81_759+82del
NM_001302552.3:c.750+81_750+82del	NP_001289481.1:n.750+81_750+82del
NM_001324195.2:c.759+81_759+82del	NP_001311124.1:n.759+81_759+82del
NR_136716.2:n.909_910del
NR_136717.2:n.908+81_908+82del
NR_136718.2:n.989_990del
NR_136719.2:n.779_780del
NR_136720.2:n.909_910del
NR_136721.2:n.828+81_828+82del