Canonical Allele Identifier: CA414983327

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15025643A>C (hg19) ; chrY:g.12913731A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12913731A>C , CM000686.2:g.12913731A>C	GRCh38
NC_000024.9:g.15025643A>C , CM000686.1:g.15025643A>C	GRCh37
NC_000024.8:g.13535037A>C	NCBI36
NG_012831.1:g.14625A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.551A>C MANE Select	ENSP00000336725.3:p.Asp184Ala
ENST00000336079.7:c.551A>C	ENSP00000336725.3:p.Asp184Ala
ENST00000360160.8:c.551A>C	ENSP00000353284.4:p.Asp184Ala
ENST00000440554.1:c.542A>C	ENSP00000400377.1:p.Asp181Ala
ENST00000454054.5:c.551A>C	ENSP00000398953.1:p.Asp184Ala
ENST00000463199.1:n.69A>C
ENST00000469101.1:n.437A>C
ENST00000472510.5:n.114A>C
NM_001122665.2:c.551A>C	NP_001116137.1:p.Asp184Ala
NM_001302552.1:c.542A>C	NP_001289481.1:p.Asp181Ala
NM_004660.4:c.551A>C	NP_004651.2:p.Asp184Ala
XM_006724878.1:c.551A>C	XP_006724941.1:p.Asp184Ala
XM_011531471.1:c.551A>C	XP_011529773.1:p.Asp184Ala
NM_001122665.3:c.551A>C	NP_001116137.1:p.Asp184Ala
NM_001302552.2:c.542A>C	NP_001289481.1:p.Asp181Ala
NM_001324195.1:c.551A>C	NP_001311124.1:p.Asp184Ala
NR_136716.1:n.702A>C
NR_136717.1:n.782A>C
NR_136718.1:n.782A>C
NR_136719.1:n.572A>C
NR_136720.1:n.702A>C
NR_136721.1:n.630A>C
NR_136722.1:n.697A>C
NR_136723.1:n.697A>C
NR_136724.1:n.617A>C
XR_001756014.2:n.655A>C
NM_004660.5:c.551A>C MANE Select	NP_004651.2:p.Asp184Ala
NM_001302552.3:c.542A>C	NP_001289481.1:p.Asp181Ala
NM_001324195.2:c.551A>C	NP_001311124.1:p.Asp184Ala
NR_136716.2:n.620A>C
NR_136717.2:n.700A>C
NR_136718.2:n.700A>C
NR_136719.2:n.490A>C
NR_136720.2:n.620A>C
NR_136721.2:n.620A>C