Canonical Allele Identifier: CA2579748441

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914863A>T , CM000686.2:g.12914863A>T	GRCh38
NC_000024.9:g.15026775A>T , CM000686.1:g.15026775A>T	GRCh37
NC_000024.8:g.13536169A>T	NCBI36
NG_012831.1:g.15757A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.760-21A>T MANE Select	ENSP00000336725.3:n.760-21A>T
ENST00000336079.7:c.760-21A>T	ENSP00000336725.3:n.760-21A>T
ENST00000360160.8:c.760-21A>T	ENSP00000353284.4:n.760-21A>T
ENST00000463199.1:n.278-21A>T
ENST00000472510.5:n.536A>T
NM_001122665.2:c.760-21A>T	NP_001116137.1:n.760-21A>T
NM_001302552.1:c.751-21A>T	NP_001289481.1:n.751-21A>T
NM_004660.4:c.760-21A>T	NP_004651.2:n.760-21A>T
XM_006724878.1:c.760-21A>T	XP_006724941.1:n.760-21A>T
XM_011531471.1:c.760-21A>T	XP_011529773.1:n.760-21A>T
NM_001122665.3:c.760-21A>T	NP_001116137.1:n.760-21A>T
NM_001302552.2:c.751-21A>T	NP_001289481.1:n.751-21A>T
NM_001324195.1:c.760-21A>T	NP_001311124.1:n.760-21A>T
NR_136716.1:n.1124A>T
NR_136717.1:n.991-21A>T
NR_136718.1:n.1204A>T
NR_136719.1:n.994A>T
NR_136720.1:n.1124A>T
NR_136721.1:n.839-21A>T
NR_136722.1:n.906-21A>T
NR_136723.1:n.1119A>T
NR_136724.1:n.1039A>T
XR_001756014.2:n.864-21A>T
NM_004660.5:c.760-21A>T MANE Select	NP_004651.2:n.760-21A>T
NM_001302552.3:c.751-21A>T	NP_001289481.1:n.751-21A>T
NM_001324195.2:c.760-21A>T	NP_001311124.1:n.760-21A>T
NR_136716.2:n.1042A>T
NR_136717.2:n.909-21A>T
NR_136718.2:n.1122A>T
NR_136719.2:n.912A>T
NR_136720.2:n.1042A>T
NR_136721.2:n.829-21A>T