Canonical Allele Identifier: CA2766242936
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12905607_12905608insA , CM000686.2:g.12905607_12905608insA GRCh38
NC_000024.9:g.15017518_15017519insA , CM000686.1:g.15017518_15017519insA GRCh37
NC_000024.8:g.13526912_13526913insA NCBI36
NG_012831.1:g.6500_6501insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.45+626_45+627insA MANE Select ENSP00000336725.3:n.45+626_45+627insA
ENST00000336079.7:c.45+626_45+627insA ENSP00000336725.3:n.45+626_45+627insA
ENST00000360160.8:c.45+626_45+627insA ENSP00000353284.4:n.45+626_45+627insA
ENST00000454054.5:c.45+626_45+627insA ENSP00000398953.1:n.45+626_45+627insA
ENST00000493363.1:n.133+626_133+627insA
NM_001122665.2:c.45+626_45+627insA NP_001116137.1:n.45+626_45+627insA
NM_004660.4:c.45+626_45+627insA NP_004651.2:n.45+626_45+627insA
XM_006724878.1:c.45+626_45+627insA XP_006724941.1:n.45+626_45+627insA
XM_011531471.1:c.45+626_45+627insA XP_011529773.1:n.45+626_45+627insA
NM_001122665.3:c.45+626_45+627insA NP_001116137.1:n.45+626_45+627insA
NM_001324195.1:c.45+626_45+627insA NP_001311124.1:n.45+626_45+627insA
NR_136716.1:n.196+626_196+627insA
NR_136717.1:n.196+626_196+627insA
NR_136718.1:n.196+626_196+627insA
NR_136719.1:n.196+626_196+627insA
NR_136720.1:n.196+626_196+627insA
NR_136721.1:n.124+626_124+627insA
XR_001756014.2:n.149+626_149+627insA
NM_004660.5:c.45+626_45+627insA MANE Select NP_004651.2:n.45+626_45+627insA
NM_001324195.2:c.45+626_45+627insA NP_001311124.1:n.45+626_45+627insA
NR_136716.2:n.114+626_114+627insA
NR_136717.2:n.114+626_114+627insA
NR_136718.2:n.114+626_114+627insA
NR_136719.2:n.114+626_114+627insA
NR_136720.2:n.114+626_114+627insA
NR_136721.2:n.114+626_114+627insA