Canonical Allele Identifier: CA414987467
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915704A>C , CM000686.2:g.12915704A>C GRCh38
NC_000024.9:g.15027616A>C , CM000686.1:g.15027616A>C GRCh37
NC_000024.8:g.13537010A>C NCBI36
NG_012831.1:g.16598A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.1094A>C MANE Select ENSP00000336725.3:p.Gln365Pro
ENST00000336079.7:c.1094A>C ENSP00000336725.3:p.Gln365Pro
ENST00000360160.8:c.1094A>C ENSP00000353284.4:p.Gln365Pro
ENST00000495478.1:n.209A>C
NM_001122665.2:c.1094A>C NP_001116137.1:p.Gln365Pro
NM_001302552.1:c.1085A>C NP_001289481.1:p.Gln362Pro
NM_004660.4:c.1094A>C NP_004651.2:p.Gln365Pro
XM_006724878.1:c.1094A>C XP_006724941.1:p.Gln365Pro
XM_011531471.1:c.1094A>C XP_011529773.1:p.Gln365Pro
NM_001122665.3:c.1094A>C NP_001116137.1:p.Gln365Pro
NM_001302552.2:c.1085A>C NP_001289481.1:p.Gln362Pro
NM_001324195.1:c.1094A>C NP_001311124.1:p.Gln365Pro
NR_136716.1:n.1563A>C
NR_136717.1:n.1325A>C
NR_136718.1:n.1643A>C
NR_136719.1:n.1433A>C
NR_136720.1:n.1563A>C
NR_136721.1:n.1156A>C
NR_136722.1:n.1240A>C
NR_136723.1:n.1558A>C
NR_136724.1:n.1478A>C
XR_001756014.2:n.1198A>C
NM_004660.5:c.1094A>C MANE Select NP_004651.2:p.Gln365Pro
NM_001302552.3:c.1085A>C NP_001289481.1:p.Gln362Pro
NM_001324195.2:c.1094A>C NP_001311124.1:p.Gln365Pro
NR_136716.2:n.1481A>C
NR_136717.2:n.1243A>C
NR_136718.2:n.1561A>C
NR_136719.2:n.1351A>C
NR_136720.2:n.1481A>C
NR_136721.2:n.1146A>C