Canonical Allele Identifier: CA2824889414

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914768C>G , CM000686.2:g.12914768C>G	GRCh38
NC_000024.9:g.15026680C>G , CM000686.1:g.15026680C>G	GRCh37
NC_000024.8:g.13536074C>G	NCBI36
NG_012831.1:g.15662C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.760-116C>G MANE Select	ENSP00000336725.3:n.760-116C>G
ENST00000336079.7:c.760-116C>G	ENSP00000336725.3:n.760-116C>G
ENST00000360160.8:c.760-116C>G	ENSP00000353284.4:n.760-116C>G
ENST00000463199.1:n.278-116C>G
ENST00000472510.5:n.441C>G
NM_001122665.2:c.760-116C>G	NP_001116137.1:n.760-116C>G
NM_001302552.1:c.751-116C>G	NP_001289481.1:n.751-116C>G
NM_004660.4:c.760-116C>G	NP_004651.2:n.760-116C>G
XM_006724878.1:c.760-116C>G	XP_006724941.1:n.760-116C>G
XM_011531471.1:c.760-116C>G	XP_011529773.1:n.760-116C>G
NM_001122665.3:c.760-116C>G	NP_001116137.1:n.760-116C>G
NM_001302552.2:c.751-116C>G	NP_001289481.1:n.751-116C>G
NM_001324195.1:c.760-116C>G	NP_001311124.1:n.760-116C>G
NR_136716.1:n.1029C>G
NR_136717.1:n.991-116C>G
NR_136718.1:n.1109C>G
NR_136719.1:n.899C>G
NR_136720.1:n.1029C>G
NR_136721.1:n.839-116C>G
NR_136722.1:n.906-116C>G
NR_136723.1:n.1024C>G
NR_136724.1:n.944C>G
XR_001756014.2:n.864-116C>G
NM_004660.5:c.760-116C>G MANE Select	NP_004651.2:n.760-116C>G
NM_001302552.3:c.751-116C>G	NP_001289481.1:n.751-116C>G
NM_001324195.2:c.760-116C>G	NP_001311124.1:n.760-116C>G
NR_136716.2:n.947C>G
NR_136717.2:n.909-116C>G
NR_136718.2:n.1027C>G
NR_136719.2:n.817C>G
NR_136720.2:n.947C>G
NR_136721.2:n.829-116C>G