Canonical Allele Identifier: CA520499326

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027803T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915891T>G , CM000686.2:g.12915891T>G	GRCh38
NC_000024.9:g.15027803T>G , CM000686.1:g.15027803T>G	GRCh37
NC_000024.8:g.13537197T>G	NCBI36
NG_012831.1:g.16785T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1173T>G MANE Select	ENSP00000336725.3:p.Ala391=
ENST00000336079.7:c.1173T>G	ENSP00000336725.3:p.Ala391=
ENST00000360160.8:c.1173T>G	ENSP00000353284.4:p.Ala391=
ENST00000495478.1:n.288T>G
NM_001122665.2:c.1173T>G	NP_001116137.1:p.Ala391=
NM_001302552.1:c.1164T>G	NP_001289481.1:p.Ala388=
NM_004660.4:c.1173T>G	NP_004651.2:p.Ala391=
XM_006724878.1:c.1173T>G	XP_006724941.1:p.Ala391=
XM_011531471.1:c.1173T>G	XP_011529773.1:p.Ala391=
NM_001122665.3:c.1173T>G	NP_001116137.1:p.Ala391=
NM_001302552.2:c.1164T>G	NP_001289481.1:p.Ala388=
NM_001324195.1:c.1173T>G	NP_001311124.1:p.Ala391=
NR_136716.1:n.1642T>G
NR_136717.1:n.1404T>G
NR_136718.1:n.1722T>G
NR_136719.1:n.1512T>G
NR_136720.1:n.1642T>G
NR_136721.1:n.1235T>G
NR_136722.1:n.1319T>G
NR_136723.1:n.1637T>G
NR_136724.1:n.1557T>G
XR_001756014.2:n.1277T>G
NM_004660.5:c.1173T>G MANE Select	NP_004651.2:p.Ala391=
NM_001302552.3:c.1164T>G	NP_001289481.1:p.Ala388=
NM_001324195.2:c.1173T>G	NP_001311124.1:p.Ala391=
NR_136716.2:n.1560T>G
NR_136717.2:n.1322T>G
NR_136718.2:n.1640T>G
NR_136719.2:n.1430T>G
NR_136720.2:n.1560T>G
NR_136721.2:n.1225T>G