Canonical Allele Identifier: CA2824889407
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914760_12914761del , CM000686.2:g.12914760_12914761del GRCh38
NC_000024.9:g.15026672_15026673del , CM000686.1:g.15026672_15026673del GRCh37
NC_000024.8:g.13536066_13536067del NCBI36
NG_012831.1:g.15654_15655del

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.759+111_759+112del MANE Select ENSP00000336725.3:n.759+111_759+112del
ENST00000336079.7:c.759+111_759+112del ENSP00000336725.3:n.759+111_759+112del
ENST00000360160.8:c.759+111_759+112del ENSP00000353284.4:n.759+111_759+112del
ENST00000463199.1:n.277+111_277+112del
ENST00000472510.5:n.433_434del
NM_001122665.2:c.759+111_759+112del NP_001116137.1:n.759+111_759+112del
NM_001302552.1:c.750+111_750+112del NP_001289481.1:n.750+111_750+112del
NM_004660.4:c.759+111_759+112del NP_004651.2:n.759+111_759+112del
XM_006724878.1:c.759+111_759+112del XP_006724941.1:n.759+111_759+112del
XM_011531471.1:c.759+111_759+112del XP_011529773.1:n.759+111_759+112del
NM_001122665.3:c.759+111_759+112del NP_001116137.1:n.759+111_759+112del
NM_001302552.2:c.750+111_750+112del NP_001289481.1:n.750+111_750+112del
NM_001324195.1:c.759+111_759+112del NP_001311124.1:n.759+111_759+112del
NR_136716.1:n.1021_1022del
NR_136717.1:n.990+111_990+112del
NR_136718.1:n.1101_1102del
NR_136719.1:n.891_892del
NR_136720.1:n.1021_1022del
NR_136721.1:n.838+111_838+112del
NR_136722.1:n.905+111_905+112del
NR_136723.1:n.1016_1017del
NR_136724.1:n.936_937del
XR_001756014.2:n.863+111_863+112del
NM_004660.5:c.759+111_759+112del MANE Select NP_004651.2:n.759+111_759+112del
NM_001302552.3:c.750+111_750+112del NP_001289481.1:n.750+111_750+112del
NM_001324195.2:c.759+111_759+112del NP_001311124.1:n.759+111_759+112del
NR_136716.2:n.939_940del
NR_136717.2:n.908+111_908+112del
NR_136718.2:n.1019_1020del
NR_136719.2:n.809_810del
NR_136720.2:n.939_940del
NR_136721.2:n.828+111_828+112del