Canonical Allele Identifier: CA2579748432

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914665_12914666del , CM000686.2:g.12914665_12914666del	GRCh38
NC_000024.9:g.15026577_15026578del , CM000686.1:g.15026577_15026578del	GRCh37
NC_000024.8:g.13535971_13535972del	NCBI36
NG_012831.1:g.15559_15560del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.759+16_759+17del MANE Select	ENSP00000336725.3:n.759+16_759+17del
ENST00000336079.7:c.759+16_759+17del	ENSP00000336725.3:n.759+16_759+17del
ENST00000360160.8:c.759+16_759+17del	ENSP00000353284.4:n.759+16_759+17del
ENST00000463199.1:n.277+16_277+17del
ENST00000472510.5:n.338_339del
NM_001122665.2:c.759+16_759+17del	NP_001116137.1:n.759+16_759+17del
NM_001302552.1:c.750+16_750+17del	NP_001289481.1:n.750+16_750+17del
NM_004660.4:c.759+16_759+17del	NP_004651.2:n.759+16_759+17del
XM_006724878.1:c.759+16_759+17del	XP_006724941.1:n.759+16_759+17del
XM_011531471.1:c.759+16_759+17del	XP_011529773.1:n.759+16_759+17del
NM_001122665.3:c.759+16_759+17del	NP_001116137.1:n.759+16_759+17del
NM_001302552.2:c.750+16_750+17del	NP_001289481.1:n.750+16_750+17del
NM_001324195.1:c.759+16_759+17del	NP_001311124.1:n.759+16_759+17del
NR_136716.1:n.926_927del
NR_136717.1:n.990+16_990+17del
NR_136718.1:n.1006_1007del
NR_136719.1:n.796_797del
NR_136720.1:n.926_927del
NR_136721.1:n.838+16_838+17del
NR_136722.1:n.905+16_905+17del
NR_136723.1:n.921_922del
NR_136724.1:n.841_842del
XR_001756014.2:n.863+16_863+17del
NM_004660.5:c.759+16_759+17del MANE Select	NP_004651.2:n.759+16_759+17del
NM_001302552.3:c.750+16_750+17del	NP_001289481.1:n.750+16_750+17del
NM_001324195.2:c.759+16_759+17del	NP_001311124.1:n.759+16_759+17del
NR_136716.2:n.844_845del
NR_136717.2:n.908+16_908+17del
NR_136718.2:n.924_925del
NR_136719.2:n.714_715del
NR_136720.2:n.844_845del
NR_136721.2:n.828+16_828+17del