Canonical Allele Identifier: CA2824889401

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914746_12914747insG , CM000686.2:g.12914746_12914747insG	GRCh38
NC_000024.9:g.15026658_15026659insG , CM000686.1:g.15026658_15026659insG	GRCh37
NC_000024.8:g.13536052_13536053insG	NCBI36
NG_012831.1:g.15640_15641insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.759+97_759+98insG MANE Select	ENSP00000336725.3:n.759+97_759+98insG
ENST00000336079.7:c.759+97_759+98insG	ENSP00000336725.3:n.759+97_759+98insG
ENST00000360160.8:c.759+97_759+98insG	ENSP00000353284.4:n.759+97_759+98insG
ENST00000463199.1:n.277+97_277+98insG
ENST00000472510.5:n.419_420insG
NM_001122665.2:c.759+97_759+98insG	NP_001116137.1:n.759+97_759+98insG
NM_001302552.1:c.750+97_750+98insG	NP_001289481.1:n.750+97_750+98insG
NM_004660.4:c.759+97_759+98insG	NP_004651.2:n.759+97_759+98insG
XM_006724878.1:c.759+97_759+98insG	XP_006724941.1:n.759+97_759+98insG
XM_011531471.1:c.759+97_759+98insG	XP_011529773.1:n.759+97_759+98insG
NM_001122665.3:c.759+97_759+98insG	NP_001116137.1:n.759+97_759+98insG
NM_001302552.2:c.750+97_750+98insG	NP_001289481.1:n.750+97_750+98insG
NM_001324195.1:c.759+97_759+98insG	NP_001311124.1:n.759+97_759+98insG
NR_136716.1:n.1007_1008insG
NR_136717.1:n.990+97_990+98insG
NR_136718.1:n.1087_1088insG
NR_136719.1:n.877_878insG
NR_136720.1:n.1007_1008insG
NR_136721.1:n.838+97_838+98insG
NR_136722.1:n.905+97_905+98insG
NR_136723.1:n.1002_1003insG
NR_136724.1:n.922_923insG
XR_001756014.2:n.863+97_863+98insG
NM_004660.5:c.759+97_759+98insG MANE Select	NP_004651.2:n.759+97_759+98insG
NM_001302552.3:c.750+97_750+98insG	NP_001289481.1:n.750+97_750+98insG
NM_001324195.2:c.759+97_759+98insG	NP_001311124.1:n.759+97_759+98insG
NR_136716.2:n.925_926insG
NR_136717.2:n.908+97_908+98insG
NR_136718.2:n.1005_1006insG
NR_136719.2:n.795_796insG
NR_136720.2:n.925_926insG
NR_136721.2:n.828+97_828+98insG