Canonical Allele Identifier: CA414987636
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915735C>A , CM000686.2:g.12915735C>A GRCh38
NC_000024.9:g.15027647C>A , CM000686.1:g.15027647C>A GRCh37
NC_000024.8:g.13537041C>A NCBI36
NG_012831.1:g.16629C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.1125C>A MANE Select ENSP00000336725.3:p.His375Gln
ENST00000336079.7:c.1125C>A ENSP00000336725.3:p.His375Gln
ENST00000360160.8:c.1125C>A ENSP00000353284.4:p.His375Gln
ENST00000495478.1:n.240C>A
NM_001122665.2:c.1125C>A NP_001116137.1:p.His375Gln
NM_001302552.1:c.1116C>A NP_001289481.1:p.His372Gln
NM_004660.4:c.1125C>A NP_004651.2:p.His375Gln
XM_006724878.1:c.1125C>A XP_006724941.1:p.His375Gln
XM_011531471.1:c.1125C>A XP_011529773.1:p.His375Gln
NM_001122665.3:c.1125C>A NP_001116137.1:p.His375Gln
NM_001302552.2:c.1116C>A NP_001289481.1:p.His372Gln
NM_001324195.1:c.1125C>A NP_001311124.1:p.His375Gln
NR_136716.1:n.1594C>A
NR_136717.1:n.1356C>A
NR_136718.1:n.1674C>A
NR_136719.1:n.1464C>A
NR_136720.1:n.1594C>A
NR_136721.1:n.1187C>A
NR_136722.1:n.1271C>A
NR_136723.1:n.1589C>A
NR_136724.1:n.1509C>A
XR_001756014.2:n.1229C>A
NM_004660.5:c.1125C>A MANE Select NP_004651.2:p.His375Gln
NM_001302552.3:c.1116C>A NP_001289481.1:p.His372Gln
NM_001324195.2:c.1125C>A NP_001311124.1:p.His375Gln
NR_136716.2:n.1512C>A
NR_136717.2:n.1274C>A
NR_136718.2:n.1592C>A
NR_136719.2:n.1382C>A
NR_136720.2:n.1512C>A
NR_136721.2:n.1177C>A