Canonical Allele Identifier: CA2470565173
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12917488A= , CM000686.2:g.12917488A= GRCh38
NC_000024.9:g.15029400A= , CM000686.1:g.15029400A= GRCh37
NC_000024.8:g.13538794A= NCBI36
NG_012831.1:g.18382A=

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.1849A= MANE Select ENSP00000336725.3:p.Ser617=
ENST00000336079.7:c.1849A= ENSP00000336725.3:p.Ser617=
ENST00000360160.8:c.1849A= ENSP00000353284.4:p.Ser617=
NM_001122665.2:c.1849A= NP_001116137.1:p.Ser617=
NM_001302552.1:c.1840A= NP_001289481.1:p.Ser614=
NM_004660.4:c.1849A= NP_004651.2:p.Ser617=
XM_006724878.1:c.1780A= XP_006724941.1:p.Ser594=
NM_001122665.3:c.1849A= NP_001116137.1:p.Ser617=
NM_001302552.2:c.1840A= NP_001289481.1:p.Ser614=
NM_001324195.1:c.1780A= NP_001311124.1:p.Ser594=
NR_136716.1:n.2318A=
NR_136717.1:n.2080A=
NR_136718.1:n.2398A=
NR_136719.1:n.2188A=
NR_136720.1:n.2249A=
NR_136721.1:n.1911A=
NR_136722.1:n.1995A=
NR_136723.1:n.2313A=
NR_136724.1:n.2233A=
XR_001756014.2:n.2013A=
NM_004660.5:c.1849A= MANE Select NP_004651.2:p.Ser617=
NM_001302552.3:c.1840A= NP_001289481.1:p.Ser614=
NM_001324195.2:c.1780A= NP_001311124.1:p.Ser594=
NR_136716.2:n.2236A=
NR_136717.2:n.1998A=
NR_136718.2:n.2316A=
NR_136719.2:n.2106A=
NR_136720.2:n.2167A=
NR_136721.2:n.1901A=