Canonical Allele Identifier: CA414987121
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915644A>G , CM000686.2:g.12915644A>G GRCh38
NC_000024.9:g.15027556A>G , CM000686.1:g.15027556A>G GRCh37
NC_000024.8:g.13536950A>G NCBI36
NG_012831.1:g.16538A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.1034A>G MANE Select ENSP00000336725.3:p.Asp345Gly
ENST00000336079.7:c.1034A>G ENSP00000336725.3:p.Asp345Gly
ENST00000360160.8:c.1034A>G ENSP00000353284.4:p.Asp345Gly
ENST00000495478.1:n.149A>G
NM_001122665.2:c.1034A>G NP_001116137.1:p.Asp345Gly
NM_001302552.1:c.1025A>G NP_001289481.1:p.Asp342Gly
NM_004660.4:c.1034A>G NP_004651.2:p.Asp345Gly
XM_006724878.1:c.1034A>G XP_006724941.1:p.Asp345Gly
XM_011531471.1:c.1034A>G XP_011529773.1:p.Asp345Gly
NM_001122665.3:c.1034A>G NP_001116137.1:p.Asp345Gly
NM_001302552.2:c.1025A>G NP_001289481.1:p.Asp342Gly
NM_001324195.1:c.1034A>G NP_001311124.1:p.Asp345Gly
NR_136716.1:n.1503A>G
NR_136717.1:n.1265A>G
NR_136718.1:n.1583A>G
NR_136719.1:n.1373A>G
NR_136720.1:n.1503A>G
NR_136721.1:n.1096A>G
NR_136722.1:n.1180A>G
NR_136723.1:n.1498A>G
NR_136724.1:n.1418A>G
XR_001756014.2:n.1138A>G
NM_004660.5:c.1034A>G MANE Select NP_004651.2:p.Asp345Gly
NM_001302552.3:c.1025A>G NP_001289481.1:p.Asp342Gly
NM_001324195.2:c.1034A>G NP_001311124.1:p.Asp345Gly
NR_136716.2:n.1421A>G
NR_136717.2:n.1183A>G
NR_136718.2:n.1501A>G
NR_136719.2:n.1291A>G
NR_136720.2:n.1421A>G
NR_136721.2:n.1086A>G