Canonical Allele Identifier: CA337722180

Gene: DDX3Y

Linked Data

• dbSNP Id: rs13447365
• gnomAD v3: Y-12910554-T-G
• gnomAD v4: Y-12910554-T-G
• MyVariant Identifiers: chrY:g.15022465T>G (hg19) ; chrY:g.12910554T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12910554T>G , CM000686.2:g.12910554T>G	GRCh38
NC_000024.9:g.15022465T>G , CM000686.1:g.15022465T>G	GRCh37
NC_000024.8:g.13531859T>G	NCBI36
NG_012831.1:g.11447T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.151+1147T>G MANE Select	ENSP00000336725.3:n.151+1147T>G
ENST00000336079.7:c.151+1147T>G	ENSP00000336725.3:n.151+1147T>G
ENST00000360160.8:c.151+1147T>G	ENSP00000353284.4:n.151+1147T>G
ENST00000440554.1:c.142+1147T>G	ENSP00000400377.1:n.142+1147T>G
ENST00000454054.5:c.151+1147T>G	ENSP00000398953.1:n.151+1147T>G
NM_001122665.2:c.151+1147T>G	NP_001116137.1:n.151+1147T>G
NM_001302552.1:c.142+1147T>G	NP_001289481.1:n.142+1147T>G
NM_004660.4:c.151+1147T>G	NP_004651.2:n.151+1147T>G
XM_006724878.1:c.151+1147T>G	XP_006724941.1:n.151+1147T>G
XM_011531471.1:c.151+1147T>G	XP_011529773.1:n.151+1147T>G
NM_001122665.3:c.151+1147T>G	NP_001116137.1:n.151+1147T>G
NM_001302552.2:c.142+1147T>G	NP_001289481.1:n.142+1147T>G
NM_001324195.1:c.151+1147T>G	NP_001311124.1:n.151+1147T>G
NR_136716.1:n.302+1147T>G
NR_136717.1:n.302+1147T>G
NR_136718.1:n.302+1147T>G
NR_136719.1:n.302+1147T>G
NR_136720.1:n.302+1147T>G
NR_136721.1:n.230+1147T>G
NR_136722.1:n.217+1147T>G
NR_136723.1:n.217+1147T>G
NR_136724.1:n.217+1147T>G
XR_001756014.2:n.255+1147T>G
NM_004660.5:c.151+1147T>G MANE Select	NP_004651.2:n.151+1147T>G
NM_001302552.3:c.142+1147T>G	NP_001289481.1:n.142+1147T>G
NM_001324195.2:c.151+1147T>G	NP_001311124.1:n.151+1147T>G
NR_136716.2:n.220+1147T>G
NR_136717.2:n.220+1147T>G
NR_136718.2:n.220+1147T>G
NR_136719.2:n.220+1147T>G
NR_136720.2:n.220+1147T>G
NR_136721.2:n.220+1147T>G