Canonical Allele Identifier: CA2766243431
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914719A>G , CM000686.2:g.12914719A>G GRCh38
NC_000024.9:g.15026631A>G , CM000686.1:g.15026631A>G GRCh37
NC_000024.8:g.13536025A>G NCBI36
NG_012831.1:g.15613A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.759+70A>G MANE Select ENSP00000336725.3:n.759+70A>G
ENST00000336079.7:c.759+70A>G ENSP00000336725.3:n.759+70A>G
ENST00000360160.8:c.759+70A>G ENSP00000353284.4:n.759+70A>G
ENST00000463199.1:n.277+70A>G
ENST00000472510.5:n.392A>G
NM_001122665.2:c.759+70A>G NP_001116137.1:n.759+70A>G
NM_001302552.1:c.750+70A>G NP_001289481.1:n.750+70A>G
NM_004660.4:c.759+70A>G NP_004651.2:n.759+70A>G
XM_006724878.1:c.759+70A>G XP_006724941.1:n.759+70A>G
XM_011531471.1:c.759+70A>G XP_011529773.1:n.759+70A>G
NM_001122665.3:c.759+70A>G NP_001116137.1:n.759+70A>G
NM_001302552.2:c.750+70A>G NP_001289481.1:n.750+70A>G
NM_001324195.1:c.759+70A>G NP_001311124.1:n.759+70A>G
NR_136716.1:n.980A>G
NR_136717.1:n.990+70A>G
NR_136718.1:n.1060A>G
NR_136719.1:n.850A>G
NR_136720.1:n.980A>G
NR_136721.1:n.838+70A>G
NR_136722.1:n.905+70A>G
NR_136723.1:n.975A>G
NR_136724.1:n.895A>G
XR_001756014.2:n.863+70A>G
NM_004660.5:c.759+70A>G MANE Select NP_004651.2:n.759+70A>G
NM_001302552.3:c.750+70A>G NP_001289481.1:n.750+70A>G
NM_001324195.2:c.759+70A>G NP_001311124.1:n.759+70A>G
NR_136716.2:n.898A>G
NR_136717.2:n.908+70A>G
NR_136718.2:n.978A>G
NR_136719.2:n.768A>G
NR_136720.2:n.898A>G
NR_136721.2:n.828+70A>G