Canonical Allele Identifier: CA414992684

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029403A>C (hg19) ; chrY:g.12917491A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917491A>C , CM000686.2:g.12917491A>C	GRCh38
NC_000024.9:g.15029403A>C , CM000686.1:g.15029403A>C	GRCh37
NC_000024.8:g.13538797A>C	NCBI36
NG_012831.1:g.18385A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1852A>C MANE Select	ENSP00000336725.3:p.Ser618Arg
ENST00000336079.7:c.1852A>C	ENSP00000336725.3:p.Ser618Arg
ENST00000360160.8:c.1852A>C	ENSP00000353284.4:p.Ser618Arg
NM_001122665.2:c.1852A>C	NP_001116137.1:p.Ser618Arg
NM_001302552.1:c.1843A>C	NP_001289481.1:p.Ser615Arg
NM_004660.4:c.1852A>C	NP_004651.2:p.Ser618Arg
XM_006724878.1:c.1783A>C	XP_006724941.1:p.Ser595Arg
NM_001122665.3:c.1852A>C	NP_001116137.1:p.Ser618Arg
NM_001302552.2:c.1843A>C	NP_001289481.1:p.Ser615Arg
NM_001324195.1:c.1783A>C	NP_001311124.1:p.Ser595Arg
NR_136716.1:n.2321A>C
NR_136717.1:n.2083A>C
NR_136718.1:n.2401A>C
NR_136719.1:n.2191A>C
NR_136720.1:n.2252A>C
NR_136721.1:n.1914A>C
NR_136722.1:n.1998A>C
NR_136723.1:n.2316A>C
NR_136724.1:n.2236A>C
XR_001756014.2:n.2016A>C
NM_004660.5:c.1852A>C MANE Select	NP_004651.2:p.Ser618Arg
NM_001302552.3:c.1843A>C	NP_001289481.1:p.Ser615Arg
NM_001324195.2:c.1783A>C	NP_001311124.1:p.Ser595Arg
NR_136716.2:n.2239A>C
NR_136717.2:n.2001A>C
NR_136718.2:n.2319A>C
NR_136719.2:n.2109A>C
NR_136720.2:n.2170A>C
NR_136721.2:n.1904A>C