Canonical Allele Identifier: CA520498227

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027563T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915651T>G , CM000686.2:g.12915651T>G	GRCh38
NC_000024.9:g.15027563T>G , CM000686.1:g.15027563T>G	GRCh37
NC_000024.8:g.13536957T>G	NCBI36
NG_012831.1:g.16545T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1041T>G MANE Select	ENSP00000336725.3:p.Ala347=
ENST00000336079.7:c.1041T>G	ENSP00000336725.3:p.Ala347=
ENST00000360160.8:c.1041T>G	ENSP00000353284.4:p.Ala347=
ENST00000495478.1:n.156T>G
NM_001122665.2:c.1041T>G	NP_001116137.1:p.Ala347=
NM_001302552.1:c.1032T>G	NP_001289481.1:p.Ala344=
NM_004660.4:c.1041T>G	NP_004651.2:p.Ala347=
XM_006724878.1:c.1041T>G	XP_006724941.1:p.Ala347=
XM_011531471.1:c.1041T>G	XP_011529773.1:p.Ala347=
NM_001122665.3:c.1041T>G	NP_001116137.1:p.Ala347=
NM_001302552.2:c.1032T>G	NP_001289481.1:p.Ala344=
NM_001324195.1:c.1041T>G	NP_001311124.1:p.Ala347=
NR_136716.1:n.1510T>G
NR_136717.1:n.1272T>G
NR_136718.1:n.1590T>G
NR_136719.1:n.1380T>G
NR_136720.1:n.1510T>G
NR_136721.1:n.1103T>G
NR_136722.1:n.1187T>G
NR_136723.1:n.1505T>G
NR_136724.1:n.1425T>G
XR_001756014.2:n.1145T>G
NM_004660.5:c.1041T>G MANE Select	NP_004651.2:p.Ala347=
NM_001302552.3:c.1032T>G	NP_001289481.1:p.Ala344=
NM_001324195.2:c.1041T>G	NP_001311124.1:p.Ala347=
NR_136716.2:n.1428T>G
NR_136717.2:n.1190T>G
NR_136718.2:n.1508T>G
NR_136719.2:n.1298T>G
NR_136720.2:n.1428T>G
NR_136721.2:n.1093T>G