Canonical Allele Identifier: CA519898659

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026798A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914886A>G , CM000686.2:g.12914886A>G	GRCh38
NC_000024.9:g.15026798A>G , CM000686.1:g.15026798A>G	GRCh37
NC_000024.8:g.13536192A>G	NCBI36
NG_012831.1:g.15780A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.762A>G MANE Select	ENSP00000336725.3:p.Glu254=
ENST00000336079.7:c.762A>G	ENSP00000336725.3:p.Glu254=
ENST00000360160.8:c.762A>G	ENSP00000353284.4:p.Glu254=
ENST00000463199.1:n.280A>G
ENST00000472510.5:n.559A>G
NM_001122665.2:c.762A>G	NP_001116137.1:p.Glu254=
NM_001302552.1:c.753A>G	NP_001289481.1:p.Glu251=
NM_004660.4:c.762A>G	NP_004651.2:p.Glu254=
XM_006724878.1:c.762A>G	XP_006724941.1:p.Glu254=
XM_011531471.1:c.762A>G	XP_011529773.1:p.Glu254=
NM_001122665.3:c.762A>G	NP_001116137.1:p.Glu254=
NM_001302552.2:c.753A>G	NP_001289481.1:p.Glu251=
NM_001324195.1:c.762A>G	NP_001311124.1:p.Glu254=
NR_136716.1:n.1147A>G
NR_136717.1:n.993A>G
NR_136718.1:n.1227A>G
NR_136719.1:n.1017A>G
NR_136720.1:n.1147A>G
NR_136721.1:n.841A>G
NR_136722.1:n.908A>G
NR_136723.1:n.1142A>G
NR_136724.1:n.1062A>G
XR_001756014.2:n.866A>G
NM_004660.5:c.762A>G MANE Select	NP_004651.2:p.Glu254=
NM_001302552.3:c.753A>G	NP_001289481.1:p.Glu251=
NM_001324195.2:c.762A>G	NP_001311124.1:p.Glu254=
NR_136716.2:n.1065A>G
NR_136717.2:n.911A>G
NR_136718.2:n.1145A>G
NR_136719.2:n.935A>G
NR_136720.2:n.1065A>G
NR_136721.2:n.831A>G