Canonical Allele Identifier: CA414983334

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15025644C>G (hg19) ; chrY:g.12913732C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12913732C>G , CM000686.2:g.12913732C>G	GRCh38
NC_000024.9:g.15025644C>G , CM000686.1:g.15025644C>G	GRCh37
NC_000024.8:g.13535038C>G	NCBI36
NG_012831.1:g.14626C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.552C>G MANE Select	ENSP00000336725.3:p.Asp184Glu
ENST00000336079.7:c.552C>G	ENSP00000336725.3:p.Asp184Glu
ENST00000360160.8:c.552C>G	ENSP00000353284.4:p.Asp184Glu
ENST00000440554.1:c.543C>G	ENSP00000400377.1:p.Asp181Glu
ENST00000454054.5:c.552C>G	ENSP00000398953.1:p.Asp184Glu
ENST00000463199.1:n.70C>G
ENST00000469101.1:n.438C>G
ENST00000472510.5:n.115C>G
NM_001122665.2:c.552C>G	NP_001116137.1:p.Asp184Glu
NM_001302552.1:c.543C>G	NP_001289481.1:p.Asp181Glu
NM_004660.4:c.552C>G	NP_004651.2:p.Asp184Glu
XM_006724878.1:c.552C>G	XP_006724941.1:p.Asp184Glu
XM_011531471.1:c.552C>G	XP_011529773.1:p.Asp184Glu
NM_001122665.3:c.552C>G	NP_001116137.1:p.Asp184Glu
NM_001302552.2:c.543C>G	NP_001289481.1:p.Asp181Glu
NM_001324195.1:c.552C>G	NP_001311124.1:p.Asp184Glu
NR_136716.1:n.703C>G
NR_136717.1:n.783C>G
NR_136718.1:n.783C>G
NR_136719.1:n.573C>G
NR_136720.1:n.703C>G
NR_136721.1:n.631C>G
NR_136722.1:n.698C>G
NR_136723.1:n.698C>G
NR_136724.1:n.618C>G
XR_001756014.2:n.656C>G
NM_004660.5:c.552C>G MANE Select	NP_004651.2:p.Asp184Glu
NM_001302552.3:c.543C>G	NP_001289481.1:p.Asp181Glu
NM_001324195.2:c.552C>G	NP_001311124.1:p.Asp184Glu
NR_136716.2:n.621C>G
NR_136717.2:n.701C>G
NR_136718.2:n.701C>G
NR_136719.2:n.491C>G
NR_136720.2:n.621C>G
NR_136721.2:n.621C>G