Canonical Allele Identifier: CA337722331
Gene: DDX3Y HGNC NCBI

Linked Data

dbSNP Id: rs2020857
gnomAD v3: Y-12918840-C-T
gnomAD v4: Y-12918840-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12918840C>T , CM000686.2:g.12918840C>T GRCh38
NC_000024.9:g.15030752C>T , CM000686.1:g.15030752C>T GRCh37
NC_000024.8:g.13540146C>T NCBI36
NG_012831.1:g.19734C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.*718C>T MANE Select ENSP00000336725.3:n.*718C>T
ENST00000336079.7:c.*718C>T ENSP00000336725.3:n.*718C>T
NM_004660.4:c.*718C>T NP_004651.2:n.*718C>T
XM_006724878.1:c.*718C>T XP_006724941.1:n.*718C>T
NM_001122665.3:c.*718C>T NP_001116137.1:n.*718C>T
NM_001302552.2:c.*718C>T NP_001289481.1:n.*718C>T
NM_001324195.1:c.*718C>T NP_001311124.1:n.*718C>T
NR_136716.1:n.3170C>T
NR_136717.1:n.2932C>T
NR_136718.1:n.3250C>T
NR_136719.1:n.3040C>T
NR_136720.1:n.3101C>T
NR_136721.1:n.2763C>T
NR_136722.1:n.2847C>T
NR_136723.1:n.3165C>T
NR_136724.1:n.3085C>T
XR_001756014.2:n.2865C>T
NM_004660.5:c.*718C>T MANE Select NP_004651.2:n.*718C>T
NM_001302552.3:c.*718C>T NP_001289481.1:n.*718C>T
NM_001324195.2:c.*718C>T NP_001311124.1:n.*718C>T
NR_136716.2:n.3088C>T
NR_136717.2:n.2850C>T
NR_136718.2:n.3168C>T
NR_136719.2:n.2958C>T
NR_136720.2:n.3019C>T
NR_136721.2:n.2753C>T