Canonical Allele Identifier: CA2470565265
Gene: DDX3Y HGNC NCBI

Linked Data

dbSNP Id: rs1603207935

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12918742C>G , CM000686.2:g.12918742C>G GRCh38
NC_000024.9:g.15030654C>G , CM000686.1:g.15030654C>G GRCh37
NC_000024.8:g.13540048C>G NCBI36
NG_012831.1:g.19636C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.*620C>G MANE Select ENSP00000336725.3:n.*620C>G
ENST00000336079.7:c.*620C>G ENSP00000336725.3:n.*620C>G
NM_004660.4:c.*620C>G NP_004651.2:n.*620C>G
XM_006724878.1:c.*620C>G XP_006724941.1:n.*620C>G
NM_001122665.3:c.*620C>G NP_001116137.1:n.*620C>G
NM_001302552.2:c.*620C>G NP_001289481.1:n.*620C>G
NM_001324195.1:c.*620C>G NP_001311124.1:n.*620C>G
NR_136716.1:n.3072C>G
NR_136717.1:n.2834C>G
NR_136718.1:n.3152C>G
NR_136719.1:n.2942C>G
NR_136720.1:n.3003C>G
NR_136721.1:n.2665C>G
NR_136722.1:n.2749C>G
NR_136723.1:n.3067C>G
NR_136724.1:n.2987C>G
XR_001756014.2:n.2767C>G
NM_004660.5:c.*620C>G MANE Select NP_004651.2:n.*620C>G
NM_001302552.3:c.*620C>G NP_001289481.1:n.*620C>G
NM_001324195.2:c.*620C>G NP_001311124.1:n.*620C>G
NR_136716.2:n.2990C>G
NR_136717.2:n.2752C>G
NR_136718.2:n.3070C>G
NR_136719.2:n.2860C>G
NR_136720.2:n.2921C>G
NR_136721.2:n.2655C>G