Canonical Allele Identifier: CA519898601

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026555T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914643T>C , CM000686.2:g.12914643T>C	GRCh38
NC_000024.9:g.15026555T>C , CM000686.1:g.15026555T>C	GRCh37
NC_000024.8:g.13535949T>C	NCBI36
NG_012831.1:g.15537T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.753T>C MANE Select	ENSP00000336725.3:p.Ala251=
ENST00000336079.7:c.753T>C	ENSP00000336725.3:p.Ala251=
ENST00000360160.8:c.753T>C	ENSP00000353284.4:p.Ala251=
ENST00000440554.1:c.744T>C	ENSP00000400377.1:p.Ala248=
ENST00000463199.1:n.271T>C
ENST00000472510.5:n.316T>C
NM_001122665.2:c.753T>C	NP_001116137.1:p.Ala251=
NM_001302552.1:c.744T>C	NP_001289481.1:p.Ala248=
NM_004660.4:c.753T>C	NP_004651.2:p.Ala251=
XM_006724878.1:c.753T>C	XP_006724941.1:p.Ala251=
XM_011531471.1:c.753T>C	XP_011529773.1:p.Ala251=
NM_001122665.3:c.753T>C	NP_001116137.1:p.Ala251=
NM_001302552.2:c.744T>C	NP_001289481.1:p.Ala248=
NM_001324195.1:c.753T>C	NP_001311124.1:p.Ala251=
NR_136716.1:n.904T>C
NR_136717.1:n.984T>C
NR_136718.1:n.984T>C
NR_136719.1:n.774T>C
NR_136720.1:n.904T>C
NR_136721.1:n.832T>C
NR_136722.1:n.899T>C
NR_136723.1:n.899T>C
NR_136724.1:n.819T>C
XR_001756014.2:n.857T>C
NM_004660.5:c.753T>C MANE Select	NP_004651.2:p.Ala251=
NM_001302552.3:c.744T>C	NP_001289481.1:p.Ala248=
NM_001324195.2:c.753T>C	NP_001311124.1:p.Ala251=
NR_136716.2:n.822T>C
NR_136717.2:n.902T>C
NR_136718.2:n.902T>C
NR_136719.2:n.692T>C
NR_136720.2:n.822T>C
NR_136721.2:n.822T>C