Canonical Allele Identifier: CA2824889420

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914857G>T , CM000686.2:g.12914857G>T	GRCh38
NC_000024.9:g.15026769G>T , CM000686.1:g.15026769G>T	GRCh37
NC_000024.8:g.13536163G>T	NCBI36
NG_012831.1:g.15751G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.760-27G>T MANE Select	ENSP00000336725.3:n.760-27G>T
ENST00000336079.7:c.760-27G>T	ENSP00000336725.3:n.760-27G>T
ENST00000360160.8:c.760-27G>T	ENSP00000353284.4:n.760-27G>T
ENST00000463199.1:n.278-27G>T
ENST00000472510.5:n.530G>T
NM_001122665.2:c.760-27G>T	NP_001116137.1:n.760-27G>T
NM_001302552.1:c.751-27G>T	NP_001289481.1:n.751-27G>T
NM_004660.4:c.760-27G>T	NP_004651.2:n.760-27G>T
XM_006724878.1:c.760-27G>T	XP_006724941.1:n.760-27G>T
XM_011531471.1:c.760-27G>T	XP_011529773.1:n.760-27G>T
NM_001122665.3:c.760-27G>T	NP_001116137.1:n.760-27G>T
NM_001302552.2:c.751-27G>T	NP_001289481.1:n.751-27G>T
NM_001324195.1:c.760-27G>T	NP_001311124.1:n.760-27G>T
NR_136716.1:n.1118G>T
NR_136717.1:n.991-27G>T
NR_136718.1:n.1198G>T
NR_136719.1:n.988G>T
NR_136720.1:n.1118G>T
NR_136721.1:n.839-27G>T
NR_136722.1:n.906-27G>T
NR_136723.1:n.1113G>T
NR_136724.1:n.1033G>T
XR_001756014.2:n.864-27G>T
NM_004660.5:c.760-27G>T MANE Select	NP_004651.2:n.760-27G>T
NM_001302552.3:c.751-27G>T	NP_001289481.1:n.751-27G>T
NM_001324195.2:c.760-27G>T	NP_001311124.1:n.760-27G>T
NR_136716.2:n.1036G>T
NR_136717.2:n.909-27G>T
NR_136718.2:n.1116G>T
NR_136719.2:n.906G>T
NR_136720.2:n.1036G>T
NR_136721.2:n.829-27G>T