Canonical Allele Identifier: CA414987786
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915759T>G , CM000686.2:g.12915759T>G GRCh38
NC_000024.9:g.15027671T>G , CM000686.1:g.15027671T>G GRCh37
NC_000024.8:g.13537065T>G NCBI36
NG_012831.1:g.16653T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.1149T>G MANE Select ENSP00000336725.3:p.Phe383Leu
ENST00000336079.7:c.1149T>G ENSP00000336725.3:p.Phe383Leu
ENST00000360160.8:c.1149T>G ENSP00000353284.4:p.Phe383Leu
ENST00000495478.1:n.264T>G
NM_001122665.2:c.1149T>G NP_001116137.1:p.Phe383Leu
NM_001302552.1:c.1140T>G NP_001289481.1:p.Phe380Leu
NM_004660.4:c.1149T>G NP_004651.2:p.Phe383Leu
XM_006724878.1:c.1149T>G XP_006724941.1:p.Phe383Leu
XM_011531471.1:c.1149T>G XP_011529773.1:p.Phe383Leu
NM_001122665.3:c.1149T>G NP_001116137.1:p.Phe383Leu
NM_001302552.2:c.1140T>G NP_001289481.1:p.Phe380Leu
NM_001324195.1:c.1149T>G NP_001311124.1:p.Phe383Leu
NR_136716.1:n.1618T>G
NR_136717.1:n.1380T>G
NR_136718.1:n.1698T>G
NR_136719.1:n.1488T>G
NR_136720.1:n.1618T>G
NR_136721.1:n.1211T>G
NR_136722.1:n.1295T>G
NR_136723.1:n.1613T>G
NR_136724.1:n.1533T>G
XR_001756014.2:n.1253T>G
NM_004660.5:c.1149T>G MANE Select NP_004651.2:p.Phe383Leu
NM_001302552.3:c.1140T>G NP_001289481.1:p.Phe380Leu
NM_001324195.2:c.1149T>G NP_001311124.1:p.Phe383Leu
NR_136716.2:n.1536T>G
NR_136717.2:n.1298T>G
NR_136718.2:n.1616T>G
NR_136719.2:n.1406T>G
NR_136720.2:n.1536T>G
NR_136721.2:n.1201T>G