Canonical Allele Identifier: CA2571589986
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12910925_12910926insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000686.2:g.12910925_12910926insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000024.9:g.15022837_15022838insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000686.1:g.15022837_15022838insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000024.8:g.13532231_13532232insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_012831.1:g.11819_11820insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000336725.3:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000336079.7:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000336725.3:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000360160.8:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000353284.4:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000440554.1:c.143-914_143-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000400377.1:n.143-914_143-913insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000454054.5:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000398953.1:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGG...
NM_001122665.2:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001116137.1:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001302552.1:c.143-914_143-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001289481.1:n.143-914_143-913insGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_004660.4:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_004651.2:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_006724878.1:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_006724941.1:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_011531471.1:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011529773.1:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001122665.3:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001116137.1:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001302552.2:c.143-914_143-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001289481.1:n.143-914_143-913insGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001324195.1:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001311124.1:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGG...
NR_136716.1:n.303-914_303-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136717.1:n.303-914_303-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136718.1:n.303-914_303-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136719.1:n.302+1518_302+1519insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136720.1:n.303-914_303-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136721.1:n.231-914_231-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136722.1:n.218-914_218-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136723.1:n.218-914_218-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136724.1:n.218-914_218-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
XR_001756014.2:n.256-914_256-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NM_004660.5:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_004651.2:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001302552.3:c.143-914_143-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001289481.1:n.143-914_143-913insGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001324195.2:c.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001311124.1:n.152-914_152-913insGGGGGGGGGGGGGGGGGGGGGGGGGG...
NR_136716.2:n.221-914_221-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136717.2:n.221-914_221-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136718.2:n.221-914_221-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136719.2:n.220+1518_220+1519insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136720.2:n.221-914_221-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NR_136721.2:n.221-914_221-913insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG