Canonical Allele Identifier: CA2766243531

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915530_12915532del , CM000686.2:g.12915530_12915532del	GRCh38
NC_000024.9:g.15027442_15027444del , CM000686.1:g.15027442_15027444del	GRCh37
NC_000024.8:g.13536836_13536838del	NCBI36
NG_012831.1:g.16424_16426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1020-100_1020-98del MANE Select	ENSP00000336725.3:n.1020-100_1020-98del
ENST00000336079.7:c.1020-100_1020-98del	ENSP00000336725.3:n.1020-100_1020-98del
ENST00000360160.8:c.1020-100_1020-98del	ENSP00000353284.4:n.1020-100_1020-98del
ENST00000495478.1:n.35_37del
NM_001122665.2:c.1020-100_1020-98del	NP_001116137.1:n.1020-100_1020-98del
NM_001302552.1:c.1011-100_1011-98del	NP_001289481.1:n.1011-100_1011-98del
NM_004660.4:c.1020-100_1020-98del	NP_004651.2:n.1020-100_1020-98del
XM_006724878.1:c.1020-100_1020-98del	XP_006724941.1:n.1020-100_1020-98del
XM_011531471.1:c.1020-100_1020-98del	XP_011529773.1:n.1020-100_1020-98del
NM_001122665.3:c.1020-100_1020-98del	NP_001116137.1:n.1020-100_1020-98del
NM_001302552.2:c.1011-100_1011-98del	NP_001289481.1:n.1011-100_1011-98del
NM_001324195.1:c.1020-100_1020-98del	NP_001311124.1:n.1020-100_1020-98del
NR_136716.1:n.1489-100_1489-98del
NR_136717.1:n.1251-100_1251-98del
NR_136718.1:n.1569-100_1569-98del
NR_136719.1:n.1359-100_1359-98del
NR_136720.1:n.1489-100_1489-98del
NR_136721.1:n.1082-100_1082-98del
NR_136722.1:n.1166-100_1166-98del
NR_136723.1:n.1484-100_1484-98del
NR_136724.1:n.1404-100_1404-98del
XR_001756014.2:n.1124-100_1124-98del
NM_004660.5:c.1020-100_1020-98del MANE Select	NP_004651.2:n.1020-100_1020-98del
NM_001302552.3:c.1011-100_1011-98del	NP_001289481.1:n.1011-100_1011-98del
NM_001324195.2:c.1020-100_1020-98del	NP_001311124.1:n.1020-100_1020-98del
NR_136716.2:n.1407-100_1407-98del
NR_136717.2:n.1169-100_1169-98del
NR_136718.2:n.1487-100_1487-98del
NR_136719.2:n.1277-100_1277-98del
NR_136720.2:n.1407-100_1407-98del
NR_136721.2:n.1072-100_1072-98del