Canonical Allele Identifier: CA414987977
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915893G>T , CM000686.2:g.12915893G>T GRCh38
NC_000024.9:g.15027805G>T , CM000686.1:g.15027805G>T GRCh37
NC_000024.8:g.13537199G>T NCBI36
NG_012831.1:g.16787G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.1175G>T MANE Select ENSP00000336725.3:p.Arg392Leu
ENST00000336079.7:c.1175G>T ENSP00000336725.3:p.Arg392Leu
ENST00000360160.8:c.1175G>T ENSP00000353284.4:p.Arg392Leu
ENST00000495478.1:n.290G>T
NM_001122665.2:c.1175G>T NP_001116137.1:p.Arg392Leu
NM_001302552.1:c.1166G>T NP_001289481.1:p.Arg389Leu
NM_004660.4:c.1175G>T NP_004651.2:p.Arg392Leu
XM_006724878.1:c.1175G>T XP_006724941.1:p.Arg392Leu
XM_011531471.1:c.1175G>T XP_011529773.1:p.Arg392Leu
NM_001122665.3:c.1175G>T NP_001116137.1:p.Arg392Leu
NM_001302552.2:c.1166G>T NP_001289481.1:p.Arg389Leu
NM_001324195.1:c.1175G>T NP_001311124.1:p.Arg392Leu
NR_136716.1:n.1644G>T
NR_136717.1:n.1406G>T
NR_136718.1:n.1724G>T
NR_136719.1:n.1514G>T
NR_136720.1:n.1644G>T
NR_136721.1:n.1237G>T
NR_136722.1:n.1321G>T
NR_136723.1:n.1639G>T
NR_136724.1:n.1559G>T
XR_001756014.2:n.1279G>T
NM_004660.5:c.1175G>T MANE Select NP_004651.2:p.Arg392Leu
NM_001302552.3:c.1166G>T NP_001289481.1:p.Arg389Leu
NM_001324195.2:c.1175G>T NP_001311124.1:p.Arg392Leu
NR_136716.2:n.1562G>T
NR_136717.2:n.1324G>T
NR_136718.2:n.1642G>T
NR_136719.2:n.1432G>T
NR_136720.2:n.1562G>T
NR_136721.2:n.1227G>T