Canonical Allele Identifier: CA337722160
Gene: DDX3Y HGNC NCBI

Linked Data

dbSNP Id: rs9786025
gnomAD v3: Y-12909611-G-A
gnomAD v4: Y-12909611-G-A
MyVariant Identifiers: chrY:g.15021522G>A (hg19) chrY:g.12909611G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12909611G>A , CM000686.2:g.12909611G>A GRCh38
NC_000024.9:g.15021522G>A , CM000686.1:g.15021522G>A GRCh37
NC_000024.8:g.13530916G>A NCBI36
NG_012831.1:g.10504G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.151+204G>A MANE Select ENSP00000336725.3:n.151+204G>A
ENST00000336079.7:c.151+204G>A ENSP00000336725.3:n.151+204G>A
ENST00000360160.8:c.151+204G>A ENSP00000353284.4:n.151+204G>A
ENST00000440554.1:c.142+204G>A ENSP00000400377.1:n.142+204G>A
ENST00000454054.5:c.151+204G>A ENSP00000398953.1:n.151+204G>A
ENST00000493363.1:n.443G>A
NM_001122665.2:c.151+204G>A NP_001116137.1:n.151+204G>A
NM_001302552.1:c.142+204G>A NP_001289481.1:n.142+204G>A
NM_004660.4:c.151+204G>A NP_004651.2:n.151+204G>A
XM_006724878.1:c.151+204G>A XP_006724941.1:n.151+204G>A
XM_011531471.1:c.151+204G>A XP_011529773.1:n.151+204G>A
NM_001122665.3:c.151+204G>A NP_001116137.1:n.151+204G>A
NM_001302552.2:c.142+204G>A NP_001289481.1:n.142+204G>A
NM_001324195.1:c.151+204G>A NP_001311124.1:n.151+204G>A
NR_136716.1:n.302+204G>A
NR_136717.1:n.302+204G>A
NR_136718.1:n.302+204G>A
NR_136719.1:n.302+204G>A
NR_136720.1:n.302+204G>A
NR_136721.1:n.230+204G>A
NR_136722.1:n.217+204G>A
NR_136723.1:n.217+204G>A
NR_136724.1:n.217+204G>A
XR_001756014.2:n.255+204G>A
NM_004660.5:c.151+204G>A MANE Select NP_004651.2:n.151+204G>A
NM_001302552.3:c.142+204G>A NP_001289481.1:n.142+204G>A
NM_001324195.2:c.151+204G>A NP_001311124.1:n.151+204G>A
NR_136716.2:n.220+204G>A
NR_136717.2:n.220+204G>A
NR_136718.2:n.220+204G>A
NR_136719.2:n.220+204G>A
NR_136720.2:n.220+204G>A
NR_136721.2:n.220+204G>A
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