Canonical Allele Identifier: CA10573786

Gene: DDX3Y

Linked Data

• dbSNP Id: rs779501255
• ExAC: Y:15029489 G / GT
• gnomAD v2: Y-15029489-G-GT
• MyVariant Identifiers: chrY:g.15029489_15029490insT (hg19) ; chrY:g.12917577_12917578insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917582dup , CM000686.2:g.12917582dup	GRCh38
NC_000024.9:g.15029494dup , CM000686.1:g.15029494dup	GRCh37
NC_000024.8:g.13538888dup	NCBI36
NG_012831.1:g.18476dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1903+40dup MANE Select	ENSP00000336725.3:n.1903+40dup
ENST00000336079.7:c.1903+40dup	ENSP00000336725.3:n.1903+40dup
ENST00000360160.8:c.1903+40dup	ENSP00000353284.4:n.1903+40dup
NM_001122665.2:c.1903+40dup	NP_001116137.1:n.1903+40dup
NM_001302552.1:c.1894+40dup	NP_001289481.1:n.1894+40dup
NM_004660.4:c.1903+40dup	NP_004651.2:n.1903+40dup
XM_006724878.1:c.1834+40dup	XP_006724941.1:n.1834+40dup
NM_001122665.3:c.1903+40dup	NP_001116137.1:n.1903+40dup
NM_001302552.2:c.1894+40dup	NP_001289481.1:n.1894+40dup
NM_001324195.1:c.1834+40dup	NP_001311124.1:n.1834+40dup
NR_136716.1:n.2372+40dup
NR_136717.1:n.2134+40dup
NR_136718.1:n.2452+40dup
NR_136719.1:n.2242+40dup
NR_136720.1:n.2303+40dup
NR_136721.1:n.1965+40dup
NR_136722.1:n.2049+40dup
NR_136723.1:n.2367+40dup
NR_136724.1:n.2287+40dup
XR_001756014.2:n.2067+40dup
NM_004660.5:c.1903+40dup MANE Select	NP_004651.2:n.1903+40dup
NM_001302552.3:c.1894+40dup	NP_001289481.1:n.1894+40dup
NM_001324195.2:c.1834+40dup	NP_001311124.1:n.1834+40dup
NR_136716.2:n.2290+40dup
NR_136717.2:n.2052+40dup
NR_136718.2:n.2370+40dup
NR_136719.2:n.2160+40dup
NR_136720.2:n.2221+40dup
NR_136721.2:n.1955+40dup