Canonical Allele Identifier: CA2766243430
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914717C>G , CM000686.2:g.12914717C>G GRCh38
NC_000024.9:g.15026629C>G , CM000686.1:g.15026629C>G GRCh37
NC_000024.8:g.13536023C>G NCBI36
NG_012831.1:g.15611C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.759+68C>G MANE Select ENSP00000336725.3:n.759+68C>G
ENST00000336079.7:c.759+68C>G ENSP00000336725.3:n.759+68C>G
ENST00000360160.8:c.759+68C>G ENSP00000353284.4:n.759+68C>G
ENST00000463199.1:n.277+68C>G
ENST00000472510.5:n.390C>G
NM_001122665.2:c.759+68C>G NP_001116137.1:n.759+68C>G
NM_001302552.1:c.750+68C>G NP_001289481.1:n.750+68C>G
NM_004660.4:c.759+68C>G NP_004651.2:n.759+68C>G
XM_006724878.1:c.759+68C>G XP_006724941.1:n.759+68C>G
XM_011531471.1:c.759+68C>G XP_011529773.1:n.759+68C>G
NM_001122665.3:c.759+68C>G NP_001116137.1:n.759+68C>G
NM_001302552.2:c.750+68C>G NP_001289481.1:n.750+68C>G
NM_001324195.1:c.759+68C>G NP_001311124.1:n.759+68C>G
NR_136716.1:n.978C>G
NR_136717.1:n.990+68C>G
NR_136718.1:n.1058C>G
NR_136719.1:n.848C>G
NR_136720.1:n.978C>G
NR_136721.1:n.838+68C>G
NR_136722.1:n.905+68C>G
NR_136723.1:n.973C>G
NR_136724.1:n.893C>G
XR_001756014.2:n.863+68C>G
NM_004660.5:c.759+68C>G MANE Select NP_004651.2:n.759+68C>G
NM_001302552.3:c.750+68C>G NP_001289481.1:n.750+68C>G
NM_001324195.2:c.759+68C>G NP_001311124.1:n.759+68C>G
NR_136716.2:n.896C>G
NR_136717.2:n.908+68C>G
NR_136718.2:n.976C>G
NR_136719.2:n.766C>G
NR_136720.2:n.896C>G
NR_136721.2:n.828+68C>G