Canonical Allele Identifier: CA2824889404

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914759_12914760insTAA , CM000686.2:g.12914759_12914760insTAA	GRCh38
NC_000024.9:g.15026671_15026672insTAA , CM000686.1:g.15026671_15026672insTAA	GRCh37
NC_000024.8:g.13536065_13536066insTAA	NCBI36
NG_012831.1:g.15653_15654insTAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.759+110_759+111insTAA MANE Select	ENSP00000336725.3:n.759+110_759+111insTAA
ENST00000336079.7:c.759+110_759+111insTAA	ENSP00000336725.3:n.759+110_759+111insTAA
ENST00000360160.8:c.759+110_759+111insTAA	ENSP00000353284.4:n.759+110_759+111insTAA
ENST00000463199.1:n.277+110_277+111insTAA
ENST00000472510.5:n.432_433insTAA
NM_001122665.2:c.759+110_759+111insTAA	NP_001116137.1:n.759+110_759+111insTAA
NM_001302552.1:c.750+110_750+111insTAA	NP_001289481.1:n.750+110_750+111insTAA
NM_004660.4:c.759+110_759+111insTAA	NP_004651.2:n.759+110_759+111insTAA
XM_006724878.1:c.759+110_759+111insTAA	XP_006724941.1:n.759+110_759+111insTAA
XM_011531471.1:c.759+110_759+111insTAA	XP_011529773.1:n.759+110_759+111insTAA
NM_001122665.3:c.759+110_759+111insTAA	NP_001116137.1:n.759+110_759+111insTAA
NM_001302552.2:c.750+110_750+111insTAA	NP_001289481.1:n.750+110_750+111insTAA
NM_001324195.1:c.759+110_759+111insTAA	NP_001311124.1:n.759+110_759+111insTAA
NR_136716.1:n.1020_1021insTAA
NR_136717.1:n.990+110_990+111insTAA
NR_136718.1:n.1100_1101insTAA
NR_136719.1:n.890_891insTAA
NR_136720.1:n.1020_1021insTAA
NR_136721.1:n.838+110_838+111insTAA
NR_136722.1:n.905+110_905+111insTAA
NR_136723.1:n.1015_1016insTAA
NR_136724.1:n.935_936insTAA
XR_001756014.2:n.863+110_863+111insTAA
NM_004660.5:c.759+110_759+111insTAA MANE Select	NP_004651.2:n.759+110_759+111insTAA
NM_001302552.3:c.750+110_750+111insTAA	NP_001289481.1:n.750+110_750+111insTAA
NM_001324195.2:c.759+110_759+111insTAA	NP_001311124.1:n.759+110_759+111insTAA
NR_136716.2:n.938_939insTAA
NR_136717.2:n.908+110_908+111insTAA
NR_136718.2:n.1018_1019insTAA
NR_136719.2:n.808_809insTAA
NR_136720.2:n.938_939insTAA
NR_136721.2:n.828+110_828+111insTAA