Canonical Allele Identifier: CA414984774
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914630A>T , CM000686.2:g.12914630A>T GRCh38
NC_000024.9:g.15026542A>T , CM000686.1:g.15026542A>T GRCh37
NC_000024.8:g.13535936A>T NCBI36
NG_012831.1:g.15524A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.740A>T MANE Select ENSP00000336725.3:p.Glu247Val
ENST00000336079.7:c.740A>T ENSP00000336725.3:p.Glu247Val
ENST00000360160.8:c.740A>T ENSP00000353284.4:p.Glu247Val
ENST00000440554.1:c.731A>T ENSP00000400377.1:p.Glu244Val
ENST00000463199.1:n.258A>T
ENST00000472510.5:n.303A>T
NM_001122665.2:c.740A>T NP_001116137.1:p.Glu247Val
NM_001302552.1:c.731A>T NP_001289481.1:p.Glu244Val
NM_004660.4:c.740A>T NP_004651.2:p.Glu247Val
XM_006724878.1:c.740A>T XP_006724941.1:p.Glu247Val
XM_011531471.1:c.740A>T XP_011529773.1:p.Glu247Val
NM_001122665.3:c.740A>T NP_001116137.1:p.Glu247Val
NM_001302552.2:c.731A>T NP_001289481.1:p.Glu244Val
NM_001324195.1:c.740A>T NP_001311124.1:p.Glu247Val
NR_136716.1:n.891A>T
NR_136717.1:n.971A>T
NR_136718.1:n.971A>T
NR_136719.1:n.761A>T
NR_136720.1:n.891A>T
NR_136721.1:n.819A>T
NR_136722.1:n.886A>T
NR_136723.1:n.886A>T
NR_136724.1:n.806A>T
XR_001756014.2:n.844A>T
NM_004660.5:c.740A>T MANE Select NP_004651.2:p.Glu247Val
NM_001302552.3:c.731A>T NP_001289481.1:p.Glu244Val
NM_001324195.2:c.740A>T NP_001311124.1:p.Glu247Val
NR_136716.2:n.809A>T
NR_136717.2:n.889A>T
NR_136718.2:n.889A>T
NR_136719.2:n.679A>T
NR_136720.2:n.809A>T
NR_136721.2:n.809A>T