Canonical Allele Identifier: CA1139171804
Gene: DDX3Y HGNC NCBI

Linked Data

gnomAD v3: Y-12919582-A-G
gnomAD v4: Y-12919582-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12919582A>G , CM000686.2:g.12919582A>G GRCh38
NC_000024.9:g.15031494A>G , CM000686.1:g.15031494A>G GRCh37
NC_000024.8:g.13540888A>G NCBI36
NG_012831.1:g.20476A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.*1460A>G MANE Select ENSP00000336725.3:n.*1460A>G
ENST00000336079.7:c.*1460A>G ENSP00000336725.3:n.*1460A>G
NM_004660.4:c.*1460A>G NP_004651.2:n.*1460A>G
XM_006724878.1:c.*1460A>G XP_006724941.1:n.*1460A>G
NM_001122665.3:c.*1460A>G NP_001116137.1:n.*1460A>G
NM_001302552.2:c.*1460A>G NP_001289481.1:n.*1460A>G
NM_001324195.1:c.*1460A>G NP_001311124.1:n.*1460A>G
NR_136716.1:n.3912A>G
NR_136717.1:n.3674A>G
NR_136718.1:n.3992A>G
NR_136719.1:n.3782A>G
NR_136720.1:n.3843A>G
NR_136721.1:n.3505A>G
NR_136722.1:n.3589A>G
NR_136723.1:n.3907A>G
NR_136724.1:n.3827A>G
XR_001756014.2:n.3607A>G
NM_004660.5:c.*1460A>G MANE Select NP_004651.2:n.*1460A>G
NM_001302552.3:c.*1460A>G NP_001289481.1:n.*1460A>G
NM_001324195.2:c.*1460A>G NP_001311124.1:n.*1460A>G
NR_136716.2:n.3830A>G
NR_136717.2:n.3592A>G
NR_136718.2:n.3910A>G
NR_136719.2:n.3700A>G
NR_136720.2:n.3761A>G
NR_136721.2:n.3495A>G