Canonical Allele Identifier: CA2766243886
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12918861A>G , CM000686.2:g.12918861A>G GRCh38
NC_000024.9:g.15030773A>G , CM000686.1:g.15030773A>G GRCh37
NC_000024.8:g.13540167A>G NCBI36
NG_012831.1:g.19755A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.*739A>G MANE Select ENSP00000336725.3:n.*739A>G
ENST00000336079.7:c.*739A>G ENSP00000336725.3:n.*739A>G
NM_004660.4:c.*739A>G NP_004651.2:n.*739A>G
XM_006724878.1:c.*739A>G XP_006724941.1:n.*739A>G
NM_001122665.3:c.*739A>G NP_001116137.1:n.*739A>G
NM_001302552.2:c.*739A>G NP_001289481.1:n.*739A>G
NM_001324195.1:c.*739A>G NP_001311124.1:n.*739A>G
NR_136716.1:n.3191A>G
NR_136717.1:n.2953A>G
NR_136718.1:n.3271A>G
NR_136719.1:n.3061A>G
NR_136720.1:n.3122A>G
NR_136721.1:n.2784A>G
NR_136722.1:n.2868A>G
NR_136723.1:n.3186A>G
NR_136724.1:n.3106A>G
XR_001756014.2:n.2886A>G
NM_004660.5:c.*739A>G MANE Select NP_004651.2:n.*739A>G
NM_001302552.3:c.*739A>G NP_001289481.1:n.*739A>G
NM_001324195.2:c.*739A>G NP_001311124.1:n.*739A>G
NR_136716.2:n.3109A>G
NR_136717.2:n.2871A>G
NR_136718.2:n.3189A>G
NR_136719.2:n.2979A>G
NR_136720.2:n.3040A>G
NR_136721.2:n.2774A>G