Canonical Allele Identifier: CA1139170359
Gene: DDX3Y HGNC NCBI

Linked Data

gnomAD v3: Y-12914782-A-G
gnomAD v4: Y-12914782-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914782A>G , CM000686.2:g.12914782A>G GRCh38
NC_000024.9:g.15026694A>G , CM000686.1:g.15026694A>G GRCh37
NC_000024.8:g.13536088A>G NCBI36
NG_012831.1:g.15676A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.760-102A>G MANE Select ENSP00000336725.3:n.760-102A>G
ENST00000336079.7:c.760-102A>G ENSP00000336725.3:n.760-102A>G
ENST00000360160.8:c.760-102A>G ENSP00000353284.4:n.760-102A>G
ENST00000463199.1:n.278-102A>G
ENST00000472510.5:n.455A>G
NM_001122665.2:c.760-102A>G NP_001116137.1:n.760-102A>G
NM_001302552.1:c.751-102A>G NP_001289481.1:n.751-102A>G
NM_004660.4:c.760-102A>G NP_004651.2:n.760-102A>G
XM_006724878.1:c.760-102A>G XP_006724941.1:n.760-102A>G
XM_011531471.1:c.760-102A>G XP_011529773.1:n.760-102A>G
NM_001122665.3:c.760-102A>G NP_001116137.1:n.760-102A>G
NM_001302552.2:c.751-102A>G NP_001289481.1:n.751-102A>G
NM_001324195.1:c.760-102A>G NP_001311124.1:n.760-102A>G
NR_136716.1:n.1043A>G
NR_136717.1:n.991-102A>G
NR_136718.1:n.1123A>G
NR_136719.1:n.913A>G
NR_136720.1:n.1043A>G
NR_136721.1:n.839-102A>G
NR_136722.1:n.906-102A>G
NR_136723.1:n.1038A>G
NR_136724.1:n.958A>G
XR_001756014.2:n.864-102A>G
NM_004660.5:c.760-102A>G MANE Select NP_004651.2:n.760-102A>G
NM_001302552.3:c.751-102A>G NP_001289481.1:n.751-102A>G
NM_001324195.2:c.760-102A>G NP_001311124.1:n.760-102A>G
NR_136716.2:n.961A>G
NR_136717.2:n.909-102A>G
NR_136718.2:n.1041A>G
NR_136719.2:n.831A>G
NR_136720.2:n.961A>G
NR_136721.2:n.829-102A>G