Canonical Allele Identifier: CA414984921
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914648A>C , CM000686.2:g.12914648A>C GRCh38
NC_000024.9:g.15026560A>C , CM000686.1:g.15026560A>C GRCh37
NC_000024.8:g.13535954A>C NCBI36
NG_012831.1:g.15542A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.758A>C MANE Select ENSP00000336725.3:p.Lys253Thr
ENST00000336079.7:c.758A>C ENSP00000336725.3:p.Lys253Thr
ENST00000360160.8:c.758A>C ENSP00000353284.4:p.Lys253Thr
ENST00000440554.1:c.749A>C ENSP00000400377.1:p.Lys250Thr
ENST00000463199.1:n.276A>C
ENST00000472510.5:n.321A>C
NM_001122665.2:c.758A>C NP_001116137.1:p.Lys253Thr
NM_001302552.1:c.749A>C NP_001289481.1:p.Lys250Thr
NM_004660.4:c.758A>C NP_004651.2:p.Lys253Thr
XM_006724878.1:c.758A>C XP_006724941.1:p.Lys253Thr
XM_011531471.1:c.758A>C XP_011529773.1:p.Lys253Thr
NM_001122665.3:c.758A>C NP_001116137.1:p.Lys253Thr
NM_001302552.2:c.749A>C NP_001289481.1:p.Lys250Thr
NM_001324195.1:c.758A>C NP_001311124.1:p.Lys253Thr
NR_136716.1:n.909A>C
NR_136717.1:n.989A>C
NR_136718.1:n.989A>C
NR_136719.1:n.779A>C
NR_136720.1:n.909A>C
NR_136721.1:n.837A>C
NR_136722.1:n.904A>C
NR_136723.1:n.904A>C
NR_136724.1:n.824A>C
XR_001756014.2:n.862A>C
NM_004660.5:c.758A>C MANE Select NP_004651.2:p.Lys253Thr
NM_001302552.3:c.749A>C NP_001289481.1:p.Lys250Thr
NM_001324195.2:c.758A>C NP_001311124.1:p.Lys253Thr
NR_136716.2:n.827A>C
NR_136717.2:n.907A>C
NR_136718.2:n.907A>C
NR_136719.2:n.697A>C
NR_136720.2:n.827A>C
NR_136721.2:n.827A>C