Canonical Allele Identifier: CA414987050

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027543T>G (hg19) ; chrY:g.12915631T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915631T>G , CM000686.2:g.12915631T>G	GRCh38
NC_000024.9:g.15027543T>G , CM000686.1:g.15027543T>G	GRCh37
NC_000024.8:g.13536937T>G	NCBI36
NG_012831.1:g.16525T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1021T>G MANE Select	ENSP00000336725.3:p.Tyr341Asp
ENST00000336079.7:c.1021T>G	ENSP00000336725.3:p.Tyr341Asp
ENST00000360160.8:c.1021T>G	ENSP00000353284.4:p.Tyr341Asp
ENST00000495478.1:n.136T>G
NM_001122665.2:c.1021T>G	NP_001116137.1:p.Tyr341Asp
NM_001302552.1:c.1012T>G	NP_001289481.1:p.Tyr338Asp
NM_004660.4:c.1021T>G	NP_004651.2:p.Tyr341Asp
XM_006724878.1:c.1021T>G	XP_006724941.1:p.Tyr341Asp
XM_011531471.1:c.1021T>G	XP_011529773.1:p.Tyr341Asp
NM_001122665.3:c.1021T>G	NP_001116137.1:p.Tyr341Asp
NM_001302552.2:c.1012T>G	NP_001289481.1:p.Tyr338Asp
NM_001324195.1:c.1021T>G	NP_001311124.1:p.Tyr341Asp
NR_136716.1:n.1490T>G
NR_136717.1:n.1252T>G
NR_136718.1:n.1570T>G
NR_136719.1:n.1360T>G
NR_136720.1:n.1490T>G
NR_136721.1:n.1083T>G
NR_136722.1:n.1167T>G
NR_136723.1:n.1485T>G
NR_136724.1:n.1405T>G
XR_001756014.2:n.1125T>G
NM_004660.5:c.1021T>G MANE Select	NP_004651.2:p.Tyr341Asp
NM_001302552.3:c.1012T>G	NP_001289481.1:p.Tyr338Asp
NM_001324195.2:c.1021T>G	NP_001311124.1:p.Tyr341Asp
NR_136716.2:n.1408T>G
NR_136717.2:n.1170T>G
NR_136718.2:n.1488T>G
NR_136719.2:n.1278T>G
NR_136720.2:n.1408T>G
NR_136721.2:n.1073T>G