Canonical Allele Identifier: CA337722332
Gene: DDX3Y HGNC NCBI

Linked Data

dbSNP Id: rs13447374

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12918855T>G , CM000686.2:g.12918855T>G GRCh38
NC_000024.9:g.15030767T>G , CM000686.1:g.15030767T>G GRCh37
NC_000024.8:g.13540161T>G NCBI36
NG_012831.1:g.19749T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.*733T>G MANE Select ENSP00000336725.3:p.=
ENST00000336079.7:c.*733T>G ENSP00000336725.3:p.=
NM_004660.4:c.*733T>G NP_004651.2:p.=
XM_006724878.1:c.*733T>G XP_006724941.1:p.=
NM_001122665.3:c.*733T>G NP_001116137.1:p.=
NM_001302552.2:c.*733T>G NP_001289481.1:p.=
NM_001324195.1:c.*733T>G NP_001311124.1:p.=
NR_136716.1:n.3185T>G
NR_136717.1:n.2947T>G
NR_136718.1:n.3265T>G
NR_136719.1:n.3055T>G
NR_136720.1:n.3116T>G
NR_136721.1:n.2778T>G
NR_136722.1:n.2862T>G
NR_136723.1:n.3180T>G
NR_136724.1:n.3100T>G
XR_001756014.2:n.2880T>G
NM_004660.5:c.*733T>G MANE Select NP_004651.2:p.=
NM_001302552.3:c.*733T>G NP_001289481.1:p.=
NM_001324195.2:c.*733T>G NP_001311124.1:p.=
NR_136716.2:n.3103T>G
NR_136717.2:n.2865T>G
NR_136718.2:n.3183T>G
NR_136719.2:n.2973T>G
NR_136720.2:n.3034T>G
NR_136721.2:n.2768T>G