Canonical Allele Identifier: CA519898648

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026589del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914681del , CM000686.2:g.12914681del	GRCh38
NC_000024.9:g.15026593del , CM000686.1:g.15026593del	GRCh37
NC_000024.8:g.13535987del	NCBI36
NG_012831.1:g.15575del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.759+32del MANE Select	ENSP00000336725.3:n.759+32del
ENST00000336079.7:c.759+32del	ENSP00000336725.3:n.759+32del
ENST00000360160.8:c.759+32del	ENSP00000353284.4:n.759+32del
ENST00000463199.1:n.277+32del
ENST00000472510.5:n.354del
NM_001122665.2:c.759+32del	NP_001116137.1:n.759+32del
NM_001302552.1:c.750+32del	NP_001289481.1:n.750+32del
NM_004660.4:c.759+32del	NP_004651.2:n.759+32del
XM_006724878.1:c.759+32del	XP_006724941.1:n.759+32del
XM_011531471.1:c.759+32del	XP_011529773.1:n.759+32del
NM_001122665.3:c.759+32del	NP_001116137.1:n.759+32del
NM_001302552.2:c.750+32del	NP_001289481.1:n.750+32del
NM_001324195.1:c.759+32del	NP_001311124.1:n.759+32del
NR_136716.1:n.942del
NR_136717.1:n.990+32del
NR_136718.1:n.1022del
NR_136719.1:n.812del
NR_136720.1:n.942del
NR_136721.1:n.838+32del
NR_136722.1:n.905+32del
NR_136723.1:n.937del
NR_136724.1:n.857del
XR_001756014.2:n.863+32del
NM_004660.5:c.759+32del MANE Select	NP_004651.2:n.759+32del
NM_001302552.3:c.750+32del	NP_001289481.1:n.750+32del
NM_001324195.2:c.759+32del	NP_001311124.1:n.759+32del
NR_136716.2:n.860del
NR_136717.2:n.908+32del
NR_136718.2:n.940del
NR_136719.2:n.730del
NR_136720.2:n.860del
NR_136721.2:n.828+32del