Canonical Allele Identifier: CA519905811

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029411C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917499C>A , CM000686.2:g.12917499C>A	GRCh38
NC_000024.9:g.15029411C>A , CM000686.1:g.15029411C>A	GRCh37
NC_000024.8:g.13538805C>A	NCBI36
NG_012831.1:g.18393C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1860C>A MANE Select	ENSP00000336725.3:p.Arg620=
ENST00000336079.7:c.1860C>A	ENSP00000336725.3:p.Arg620=
ENST00000360160.8:c.1860C>A	ENSP00000353284.4:p.Arg620=
NM_001122665.2:c.1860C>A	NP_001116137.1:p.Arg620=
NM_001302552.1:c.1851C>A	NP_001289481.1:p.Arg617=
NM_004660.4:c.1860C>A	NP_004651.2:p.Arg620=
XM_006724878.1:c.1791C>A	XP_006724941.1:p.Arg597=
NM_001122665.3:c.1860C>A	NP_001116137.1:p.Arg620=
NM_001302552.2:c.1851C>A	NP_001289481.1:p.Arg617=
NM_001324195.1:c.1791C>A	NP_001311124.1:p.Arg597=
NR_136716.1:n.2329C>A
NR_136717.1:n.2091C>A
NR_136718.1:n.2409C>A
NR_136719.1:n.2199C>A
NR_136720.1:n.2260C>A
NR_136721.1:n.1922C>A
NR_136722.1:n.2006C>A
NR_136723.1:n.2324C>A
NR_136724.1:n.2244C>A
XR_001756014.2:n.2024C>A
NM_004660.5:c.1860C>A MANE Select	NP_004651.2:p.Arg620=
NM_001302552.3:c.1851C>A	NP_001289481.1:p.Arg617=
NM_001324195.2:c.1791C>A	NP_001311124.1:p.Arg597=
NR_136716.2:n.2247C>A
NR_136717.2:n.2009C>A
NR_136718.2:n.2327C>A
NR_136719.2:n.2117C>A
NR_136720.2:n.2178C>A
NR_136721.2:n.1912C>A