Canonical Allele Identifier: CA2824889402

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914757_12914759del , CM000686.2:g.12914757_12914759del	GRCh38
NC_000024.9:g.15026669_15026671del , CM000686.1:g.15026669_15026671del	GRCh37
NC_000024.8:g.13536063_13536065del	NCBI36
NG_012831.1:g.15651_15653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.759+108_759+110del MANE Select	ENSP00000336725.3:n.759+108_759+110del
ENST00000336079.7:c.759+108_759+110del	ENSP00000336725.3:n.759+108_759+110del
ENST00000360160.8:c.759+108_759+110del	ENSP00000353284.4:n.759+108_759+110del
ENST00000463199.1:n.277+108_277+110del
ENST00000472510.5:n.430_432del
NM_001122665.2:c.759+108_759+110del	NP_001116137.1:n.759+108_759+110del
NM_001302552.1:c.750+108_750+110del	NP_001289481.1:n.750+108_750+110del
NM_004660.4:c.759+108_759+110del	NP_004651.2:n.759+108_759+110del
XM_006724878.1:c.759+108_759+110del	XP_006724941.1:n.759+108_759+110del
XM_011531471.1:c.759+108_759+110del	XP_011529773.1:n.759+108_759+110del
NM_001122665.3:c.759+108_759+110del	NP_001116137.1:n.759+108_759+110del
NM_001302552.2:c.750+108_750+110del	NP_001289481.1:n.750+108_750+110del
NM_001324195.1:c.759+108_759+110del	NP_001311124.1:n.759+108_759+110del
NR_136716.1:n.1018_1020del
NR_136717.1:n.990+108_990+110del
NR_136718.1:n.1098_1100del
NR_136719.1:n.888_890del
NR_136720.1:n.1018_1020del
NR_136721.1:n.838+108_838+110del
NR_136722.1:n.905+108_905+110del
NR_136723.1:n.1013_1015del
NR_136724.1:n.933_935del
XR_001756014.2:n.863+108_863+110del
NM_004660.5:c.759+108_759+110del MANE Select	NP_004651.2:n.759+108_759+110del
NM_001302552.3:c.750+108_750+110del	NP_001289481.1:n.750+108_750+110del
NM_001324195.2:c.759+108_759+110del	NP_001311124.1:n.759+108_759+110del
NR_136716.2:n.936_938del
NR_136717.2:n.908+108_908+110del
NR_136718.2:n.1016_1018del
NR_136719.2:n.806_808del
NR_136720.2:n.936_938del
NR_136721.2:n.828+108_828+110del