Canonical Allele Identifier: CA520498188

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027557T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915645T>C , CM000686.2:g.12915645T>C	GRCh38
NC_000024.9:g.15027557T>C , CM000686.1:g.15027557T>C	GRCh37
NC_000024.8:g.13536951T>C	NCBI36
NG_012831.1:g.16539T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1035T>C MANE Select	ENSP00000336725.3:p.Asp345=
ENST00000336079.7:c.1035T>C	ENSP00000336725.3:p.Asp345=
ENST00000360160.8:c.1035T>C	ENSP00000353284.4:p.Asp345=
ENST00000495478.1:n.150T>C
NM_001122665.2:c.1035T>C	NP_001116137.1:p.Asp345=
NM_001302552.1:c.1026T>C	NP_001289481.1:p.Asp342=
NM_004660.4:c.1035T>C	NP_004651.2:p.Asp345=
XM_006724878.1:c.1035T>C	XP_006724941.1:p.Asp345=
XM_011531471.1:c.1035T>C	XP_011529773.1:p.Asp345=
NM_001122665.3:c.1035T>C	NP_001116137.1:p.Asp345=
NM_001302552.2:c.1026T>C	NP_001289481.1:p.Asp342=
NM_001324195.1:c.1035T>C	NP_001311124.1:p.Asp345=
NR_136716.1:n.1504T>C
NR_136717.1:n.1266T>C
NR_136718.1:n.1584T>C
NR_136719.1:n.1374T>C
NR_136720.1:n.1504T>C
NR_136721.1:n.1097T>C
NR_136722.1:n.1181T>C
NR_136723.1:n.1499T>C
NR_136724.1:n.1419T>C
XR_001756014.2:n.1139T>C
NM_004660.5:c.1035T>C MANE Select	NP_004651.2:p.Asp345=
NM_001302552.3:c.1026T>C	NP_001289481.1:p.Asp342=
NM_001324195.2:c.1035T>C	NP_001311124.1:p.Asp345=
NR_136716.2:n.1422T>C
NR_136717.2:n.1184T>C
NR_136718.2:n.1502T>C
NR_136719.2:n.1292T>C
NR_136720.2:n.1422T>C
NR_136721.2:n.1087T>C