Canonical Allele Identifier: CA2824889403

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914756_12914759dup , CM000686.2:g.12914756_12914759dup	GRCh38
NC_000024.9:g.15026668_15026671dup , CM000686.1:g.15026668_15026671dup	GRCh37
NC_000024.8:g.13536062_13536065dup	NCBI36
NG_012831.1:g.15650_15653dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.759+107_759+110dup MANE Select	ENSP00000336725.3:n.759+107_759+110dup
ENST00000336079.7:c.759+107_759+110dup	ENSP00000336725.3:n.759+107_759+110dup
ENST00000360160.8:c.759+107_759+110dup	ENSP00000353284.4:n.759+107_759+110dup
ENST00000463199.1:n.277+107_277+110dup
ENST00000472510.5:n.429_432dup
NM_001122665.2:c.759+107_759+110dup	NP_001116137.1:n.759+107_759+110dup
NM_001302552.1:c.750+107_750+110dup	NP_001289481.1:n.750+107_750+110dup
NM_004660.4:c.759+107_759+110dup	NP_004651.2:n.759+107_759+110dup
XM_006724878.1:c.759+107_759+110dup	XP_006724941.1:n.759+107_759+110dup
XM_011531471.1:c.759+107_759+110dup	XP_011529773.1:n.759+107_759+110dup
NM_001122665.3:c.759+107_759+110dup	NP_001116137.1:n.759+107_759+110dup
NM_001302552.2:c.750+107_750+110dup	NP_001289481.1:n.750+107_750+110dup
NM_001324195.1:c.759+107_759+110dup	NP_001311124.1:n.759+107_759+110dup
NR_136716.1:n.1017_1020dup
NR_136717.1:n.990+107_990+110dup
NR_136718.1:n.1097_1100dup
NR_136719.1:n.887_890dup
NR_136720.1:n.1017_1020dup
NR_136721.1:n.838+107_838+110dup
NR_136722.1:n.905+107_905+110dup
NR_136723.1:n.1012_1015dup
NR_136724.1:n.932_935dup
XR_001756014.2:n.863+107_863+110dup
NM_004660.5:c.759+107_759+110dup MANE Select	NP_004651.2:n.759+107_759+110dup
NM_001302552.3:c.750+107_750+110dup	NP_001289481.1:n.750+107_750+110dup
NM_001324195.2:c.759+107_759+110dup	NP_001311124.1:n.759+107_759+110dup
NR_136716.2:n.935_938dup
NR_136717.2:n.908+107_908+110dup
NR_136718.2:n.1015_1018dup
NR_136719.2:n.805_808dup
NR_136720.2:n.935_938dup
NR_136721.2:n.828+107_828+110dup