Canonical Allele Identifier: CA414985001

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026795G>A (hg19) ; chrY:g.12914883G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914883G>A , CM000686.2:g.12914883G>A	GRCh38
NC_000024.9:g.15026795G>A , CM000686.1:g.15026795G>A	GRCh37
NC_000024.8:g.13536189G>A	NCBI36
NG_012831.1:g.15777G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.760-1G>A MANE Select	ENSP00000336725.3:n.760-1G>A
ENST00000336079.7:c.760-1G>A	ENSP00000336725.3:n.760-1G>A
ENST00000360160.8:c.760-1G>A	ENSP00000353284.4:n.760-1G>A
ENST00000463199.1:n.278-1G>A
ENST00000472510.5:n.556G>A
NM_001122665.2:c.760-1G>A	NP_001116137.1:n.760-1G>A
NM_001302552.1:c.751-1G>A	NP_001289481.1:n.751-1G>A
NM_004660.4:c.760-1G>A	NP_004651.2:n.760-1G>A
XM_006724878.1:c.760-1G>A	XP_006724941.1:n.760-1G>A
XM_011531471.1:c.760-1G>A	XP_011529773.1:n.760-1G>A
NM_001122665.3:c.760-1G>A	NP_001116137.1:n.760-1G>A
NM_001302552.2:c.751-1G>A	NP_001289481.1:n.751-1G>A
NM_001324195.1:c.760-1G>A	NP_001311124.1:n.760-1G>A
NR_136716.1:n.1144G>A
NR_136717.1:n.991-1G>A
NR_136718.1:n.1224G>A
NR_136719.1:n.1014G>A
NR_136720.1:n.1144G>A
NR_136721.1:n.839-1G>A
NR_136722.1:n.906-1G>A
NR_136723.1:n.1139G>A
NR_136724.1:n.1059G>A
XR_001756014.2:n.864-1G>A
NM_004660.5:c.760-1G>A MANE Select	NP_004651.2:n.760-1G>A
NM_001302552.3:c.751-1G>A	NP_001289481.1:n.751-1G>A
NM_001324195.2:c.760-1G>A	NP_001311124.1:n.760-1G>A
NR_136716.2:n.1062G>A
NR_136717.2:n.909-1G>A
NR_136718.2:n.1142G>A
NR_136719.2:n.932G>A
NR_136720.2:n.1062G>A
NR_136721.2:n.829-1G>A