Canonical Allele Identifier: CA414987450

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027613A>T (hg19) ; chrY:g.12915701A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915701A>T , CM000686.2:g.12915701A>T	GRCh38
NC_000024.9:g.15027613A>T , CM000686.1:g.15027613A>T	GRCh37
NC_000024.8:g.13537007A>T	NCBI36
NG_012831.1:g.16595A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1091A>T MANE Select	ENSP00000336725.3:p.Glu364Val
ENST00000336079.7:c.1091A>T	ENSP00000336725.3:p.Glu364Val
ENST00000360160.8:c.1091A>T	ENSP00000353284.4:p.Glu364Val
ENST00000495478.1:n.206A>T
NM_001122665.2:c.1091A>T	NP_001116137.1:p.Glu364Val
NM_001302552.1:c.1082A>T	NP_001289481.1:p.Glu361Val
NM_004660.4:c.1091A>T	NP_004651.2:p.Glu364Val
XM_006724878.1:c.1091A>T	XP_006724941.1:p.Glu364Val
XM_011531471.1:c.1091A>T	XP_011529773.1:p.Glu364Val
NM_001122665.3:c.1091A>T	NP_001116137.1:p.Glu364Val
NM_001302552.2:c.1082A>T	NP_001289481.1:p.Glu361Val
NM_001324195.1:c.1091A>T	NP_001311124.1:p.Glu364Val
NR_136716.1:n.1560A>T
NR_136717.1:n.1322A>T
NR_136718.1:n.1640A>T
NR_136719.1:n.1430A>T
NR_136720.1:n.1560A>T
NR_136721.1:n.1153A>T
NR_136722.1:n.1237A>T
NR_136723.1:n.1555A>T
NR_136724.1:n.1475A>T
XR_001756014.2:n.1195A>T
NM_004660.5:c.1091A>T MANE Select	NP_004651.2:p.Glu364Val
NM_001302552.3:c.1082A>T	NP_001289481.1:p.Glu361Val
NM_001324195.2:c.1091A>T	NP_001311124.1:p.Glu364Val
NR_136716.2:n.1478A>T
NR_136717.2:n.1240A>T
NR_136718.2:n.1558A>T
NR_136719.2:n.1348A>T
NR_136720.2:n.1478A>T
NR_136721.2:n.1143A>T