Canonical Allele Identifier: CA414987142
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915647A>C , CM000686.2:g.12915647A>C GRCh38
NC_000024.9:g.15027559A>C , CM000686.1:g.15027559A>C GRCh37
NC_000024.8:g.13536953A>C NCBI36
NG_012831.1:g.16541A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.1037A>C MANE Select ENSP00000336725.3:p.Glu346Ala
ENST00000336079.7:c.1037A>C ENSP00000336725.3:p.Glu346Ala
ENST00000360160.8:c.1037A>C ENSP00000353284.4:p.Glu346Ala
ENST00000495478.1:n.152A>C
NM_001122665.2:c.1037A>C NP_001116137.1:p.Glu346Ala
NM_001302552.1:c.1028A>C NP_001289481.1:p.Glu343Ala
NM_004660.4:c.1037A>C NP_004651.2:p.Glu346Ala
XM_006724878.1:c.1037A>C XP_006724941.1:p.Glu346Ala
XM_011531471.1:c.1037A>C XP_011529773.1:p.Glu346Ala
NM_001122665.3:c.1037A>C NP_001116137.1:p.Glu346Ala
NM_001302552.2:c.1028A>C NP_001289481.1:p.Glu343Ala
NM_001324195.1:c.1037A>C NP_001311124.1:p.Glu346Ala
NR_136716.1:n.1506A>C
NR_136717.1:n.1268A>C
NR_136718.1:n.1586A>C
NR_136719.1:n.1376A>C
NR_136720.1:n.1506A>C
NR_136721.1:n.1099A>C
NR_136722.1:n.1183A>C
NR_136723.1:n.1501A>C
NR_136724.1:n.1421A>C
XR_001756014.2:n.1141A>C
NM_004660.5:c.1037A>C MANE Select NP_004651.2:p.Glu346Ala
NM_001302552.3:c.1028A>C NP_001289481.1:p.Glu343Ala
NM_001324195.2:c.1037A>C NP_001311124.1:p.Glu346Ala
NR_136716.2:n.1424A>C
NR_136717.2:n.1186A>C
NR_136718.2:n.1504A>C
NR_136719.2:n.1294A>C
NR_136720.2:n.1424A>C
NR_136721.2:n.1089A>C