Canonical Allele Identifier: CA2508494255

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12910885del , CM000686.2:g.12910885del	GRCh38
NC_000024.9:g.15022796del , CM000686.1:g.15022796del	GRCh37
NC_000024.8:g.13532190del	NCBI36
NG_012831.1:g.11778del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.152-954del MANE Select	ENSP00000336725.3:n.152-954del
ENST00000336079.7:c.152-954del	ENSP00000336725.3:n.152-954del
ENST00000360160.8:c.152-954del	ENSP00000353284.4:n.152-954del
ENST00000440554.1:c.143-954del	ENSP00000400377.1:n.143-954del
ENST00000454054.5:c.152-954del	ENSP00000398953.1:n.152-954del
NM_001122665.2:c.152-954del	NP_001116137.1:n.152-954del
NM_001302552.1:c.143-954del	NP_001289481.1:n.143-954del
NM_004660.4:c.152-954del	NP_004651.2:n.152-954del
XM_006724878.1:c.152-954del	XP_006724941.1:n.152-954del
XM_011531471.1:c.152-954del	XP_011529773.1:n.152-954del
NM_001122665.3:c.152-954del	NP_001116137.1:n.152-954del
NM_001302552.2:c.143-954del	NP_001289481.1:n.143-954del
NM_001324195.1:c.152-954del	NP_001311124.1:n.152-954del
NR_136716.1:n.303-954del
NR_136717.1:n.303-954del
NR_136718.1:n.303-954del
NR_136719.1:n.302+1478del
NR_136720.1:n.303-954del
NR_136721.1:n.231-954del
NR_136722.1:n.218-954del
NR_136723.1:n.218-954del
NR_136724.1:n.218-954del
XR_001756014.2:n.256-954del
NM_004660.5:c.152-954del MANE Select	NP_004651.2:n.152-954del
NM_001302552.3:c.143-954del	NP_001289481.1:n.143-954del
NM_001324195.2:c.152-954del	NP_001311124.1:n.152-954del
NR_136716.2:n.221-954del
NR_136717.2:n.221-954del
NR_136718.2:n.221-954del
NR_136719.2:n.220+1478del
NR_136720.2:n.221-954del
NR_136721.2:n.221-954del