Canonical Allele Identifier: CA414987871
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915773A>T , CM000686.2:g.12915773A>T GRCh38
NC_000024.9:g.15027685A>T , CM000686.1:g.15027685A>T GRCh37
NC_000024.8:g.13537079A>T NCBI36
NG_012831.1:g.16667A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.1163A>T MANE Select ENSP00000336725.3:p.Gln388Leu
ENST00000336079.7:c.1163A>T ENSP00000336725.3:p.Gln388Leu
ENST00000360160.8:c.1163A>T ENSP00000353284.4:p.Gln388Leu
ENST00000495478.1:n.278A>T
NM_001122665.2:c.1163A>T NP_001116137.1:p.Gln388Leu
NM_001302552.1:c.1154A>T NP_001289481.1:p.Gln385Leu
NM_004660.4:c.1163A>T NP_004651.2:p.Gln388Leu
XM_006724878.1:c.1163A>T XP_006724941.1:p.Gln388Leu
XM_011531471.1:c.1163A>T XP_011529773.1:p.Gln388Leu
NM_001122665.3:c.1163A>T NP_001116137.1:p.Gln388Leu
NM_001302552.2:c.1154A>T NP_001289481.1:p.Gln385Leu
NM_001324195.1:c.1163A>T NP_001311124.1:p.Gln388Leu
NR_136716.1:n.1632A>T
NR_136717.1:n.1394A>T
NR_136718.1:n.1712A>T
NR_136719.1:n.1502A>T
NR_136720.1:n.1632A>T
NR_136721.1:n.1225A>T
NR_136722.1:n.1309A>T
NR_136723.1:n.1627A>T
NR_136724.1:n.1547A>T
XR_001756014.2:n.1267A>T
NM_004660.5:c.1163A>T MANE Select NP_004651.2:p.Gln388Leu
NM_001302552.3:c.1154A>T NP_001289481.1:p.Gln385Leu
NM_001324195.2:c.1163A>T NP_001311124.1:p.Gln388Leu
NR_136716.2:n.1550A>T
NR_136717.2:n.1312A>T
NR_136718.2:n.1630A>T
NR_136719.2:n.1420A>T
NR_136720.2:n.1550A>T
NR_136721.2:n.1215A>T