Canonical Allele Identifier: CA414992733

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029409C>T (hg19) ; chrY:g.12917497C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917497C>T , CM000686.2:g.12917497C>T	GRCh38
NC_000024.9:g.15029409C>T , CM000686.1:g.15029409C>T	GRCh37
NC_000024.8:g.13538803C>T	NCBI36
NG_012831.1:g.18391C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1858C>T MANE Select	ENSP00000336725.3:p.Arg620Cys
ENST00000336079.7:c.1858C>T	ENSP00000336725.3:p.Arg620Cys
ENST00000360160.8:c.1858C>T	ENSP00000353284.4:p.Arg620Cys
NM_001122665.2:c.1858C>T	NP_001116137.1:p.Arg620Cys
NM_001302552.1:c.1849C>T	NP_001289481.1:p.Arg617Cys
NM_004660.4:c.1858C>T	NP_004651.2:p.Arg620Cys
XM_006724878.1:c.1789C>T	XP_006724941.1:p.Arg597Cys
NM_001122665.3:c.1858C>T	NP_001116137.1:p.Arg620Cys
NM_001302552.2:c.1849C>T	NP_001289481.1:p.Arg617Cys
NM_001324195.1:c.1789C>T	NP_001311124.1:p.Arg597Cys
NR_136716.1:n.2327C>T
NR_136717.1:n.2089C>T
NR_136718.1:n.2407C>T
NR_136719.1:n.2197C>T
NR_136720.1:n.2258C>T
NR_136721.1:n.1920C>T
NR_136722.1:n.2004C>T
NR_136723.1:n.2322C>T
NR_136724.1:n.2242C>T
XR_001756014.2:n.2022C>T
NM_004660.5:c.1858C>T MANE Select	NP_004651.2:p.Arg620Cys
NM_001302552.3:c.1849C>T	NP_001289481.1:p.Arg617Cys
NM_001324195.2:c.1789C>T	NP_001311124.1:p.Arg597Cys
NR_136716.2:n.2245C>T
NR_136717.2:n.2007C>T
NR_136718.2:n.2325C>T
NR_136719.2:n.2115C>T
NR_136720.2:n.2176C>T
NR_136721.2:n.1910C>T