Canonical Allele Identifier: CA414987306
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915675T>G , CM000686.2:g.12915675T>G GRCh38
NC_000024.9:g.15027587T>G , CM000686.1:g.15027587T>G GRCh37
NC_000024.8:g.13536981T>G NCBI36
NG_012831.1:g.16569T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.1065T>G MANE Select ENSP00000336725.3:p.Phe355Leu
ENST00000336079.7:c.1065T>G ENSP00000336725.3:p.Phe355Leu
ENST00000360160.8:c.1065T>G ENSP00000353284.4:p.Phe355Leu
ENST00000495478.1:n.180T>G
NM_001122665.2:c.1065T>G NP_001116137.1:p.Phe355Leu
NM_001302552.1:c.1056T>G NP_001289481.1:p.Phe352Leu
NM_004660.4:c.1065T>G NP_004651.2:p.Phe355Leu
XM_006724878.1:c.1065T>G XP_006724941.1:p.Phe355Leu
XM_011531471.1:c.1065T>G XP_011529773.1:p.Phe355Leu
NM_001122665.3:c.1065T>G NP_001116137.1:p.Phe355Leu
NM_001302552.2:c.1056T>G NP_001289481.1:p.Phe352Leu
NM_001324195.1:c.1065T>G NP_001311124.1:p.Phe355Leu
NR_136716.1:n.1534T>G
NR_136717.1:n.1296T>G
NR_136718.1:n.1614T>G
NR_136719.1:n.1404T>G
NR_136720.1:n.1534T>G
NR_136721.1:n.1127T>G
NR_136722.1:n.1211T>G
NR_136723.1:n.1529T>G
NR_136724.1:n.1449T>G
XR_001756014.2:n.1169T>G
NM_004660.5:c.1065T>G MANE Select NP_004651.2:p.Phe355Leu
NM_001302552.3:c.1056T>G NP_001289481.1:p.Phe352Leu
NM_001324195.2:c.1065T>G NP_001311124.1:p.Phe355Leu
NR_136716.2:n.1452T>G
NR_136717.2:n.1214T>G
NR_136718.2:n.1532T>G
NR_136719.2:n.1322T>G
NR_136720.2:n.1452T>G
NR_136721.2:n.1117T>G