Canonical Allele Identifier: CA337722334
Gene: DDX3Y HGNC NCBI

Linked Data

dbSNP Id: rs13447375

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12918966C>T , CM000686.2:g.12918966C>T GRCh38
NC_000024.9:g.15030878C>T , CM000686.1:g.15030878C>T GRCh37
NC_000024.8:g.13540272C>T NCBI36
NG_012831.1:g.19860C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.*844C>T MANE Select ENSP00000336725.3:n.*844C>T
ENST00000336079.7:c.*844C>T ENSP00000336725.3:n.*844C>T
NM_004660.4:c.*844C>T NP_004651.2:n.*844C>T
XM_006724878.1:c.*844C>T XP_006724941.1:n.*844C>T
NM_001122665.3:c.*844C>T NP_001116137.1:n.*844C>T
NM_001302552.2:c.*844C>T NP_001289481.1:n.*844C>T
NM_001324195.1:c.*844C>T NP_001311124.1:n.*844C>T
NR_136716.1:n.3296C>T
NR_136717.1:n.3058C>T
NR_136718.1:n.3376C>T
NR_136719.1:n.3166C>T
NR_136720.1:n.3227C>T
NR_136721.1:n.2889C>T
NR_136722.1:n.2973C>T
NR_136723.1:n.3291C>T
NR_136724.1:n.3211C>T
XR_001756014.2:n.2991C>T
NM_004660.5:c.*844C>T MANE Select NP_004651.2:n.*844C>T
NM_001302552.3:c.*844C>T NP_001289481.1:n.*844C>T
NM_001324195.2:c.*844C>T NP_001311124.1:n.*844C>T
NR_136716.2:n.3214C>T
NR_136717.2:n.2976C>T
NR_136718.2:n.3294C>T
NR_136719.2:n.3084C>T
NR_136720.2:n.3145C>T
NR_136721.2:n.2879C>T