Canonical Allele Identifier: CA414984430

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026497T>G (hg19) ; chrY:g.12914585T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914585T>G , CM000686.2:g.12914585T>G	GRCh38
NC_000024.9:g.15026497T>G , CM000686.1:g.15026497T>G	GRCh37
NC_000024.8:g.13535891T>G	NCBI36
NG_012831.1:g.15479T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.695T>G MANE Select	ENSP00000336725.3:p.Phe232Cys
ENST00000336079.7:c.695T>G	ENSP00000336725.3:p.Phe232Cys
ENST00000360160.8:c.695T>G	ENSP00000353284.4:p.Phe232Cys
ENST00000440554.1:c.686T>G	ENSP00000400377.1:p.Phe229Cys
ENST00000463199.1:n.213T>G
ENST00000472510.5:n.258T>G
NM_001122665.2:c.695T>G	NP_001116137.1:p.Phe232Cys
NM_001302552.1:c.686T>G	NP_001289481.1:p.Phe229Cys
NM_004660.4:c.695T>G	NP_004651.2:p.Phe232Cys
XM_006724878.1:c.695T>G	XP_006724941.1:p.Phe232Cys
XM_011531471.1:c.695T>G	XP_011529773.1:p.Phe232Cys
NM_001122665.3:c.695T>G	NP_001116137.1:p.Phe232Cys
NM_001302552.2:c.686T>G	NP_001289481.1:p.Phe229Cys
NM_001324195.1:c.695T>G	NP_001311124.1:p.Phe232Cys
NR_136716.1:n.846T>G
NR_136717.1:n.926T>G
NR_136718.1:n.926T>G
NR_136719.1:n.716T>G
NR_136720.1:n.846T>G
NR_136721.1:n.774T>G
NR_136722.1:n.841T>G
NR_136723.1:n.841T>G
NR_136724.1:n.761T>G
XR_001756014.2:n.799T>G
NM_004660.5:c.695T>G MANE Select	NP_004651.2:p.Phe232Cys
NM_001302552.3:c.686T>G	NP_001289481.1:p.Phe229Cys
NM_001324195.2:c.695T>G	NP_001311124.1:p.Phe232Cys
NR_136716.2:n.764T>G
NR_136717.2:n.844T>G
NR_136718.2:n.844T>G
NR_136719.2:n.634T>G
NR_136720.2:n.764T>G
NR_136721.2:n.764T>G