Canonical Allele Identifier: CA10573711

Gene: DDX3Y

Linked Data

• dbSNP Id: rs755508141
• ExAC: Y:15027720 AT / A
• gnomAD v2: Y-15027720-AT-A
• gnomAD v3: Y-12915808-AT-A
• gnomAD v4: Y-12915808-AT-A
• MyVariant Identifiers: chrY:g.15027721del (hg19) ; chrY:g.12915810del (hg38) ; chrY:g.12915809del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915811del , CM000686.2:g.12915811del	GRCh38
NC_000024.9:g.15027723del , CM000686.1:g.15027723del	GRCh37
NC_000024.8:g.13537117del	NCBI36
NG_012831.1:g.16705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1164+37del MANE Select	ENSP00000336725.3:n.1164+37del
ENST00000336079.7:c.1164+37del	ENSP00000336725.3:n.1164+37del
ENST00000360160.8:c.1164+37del	ENSP00000353284.4:n.1164+37del
ENST00000495478.1:n.279+37del
NM_001122665.2:c.1164+37del	NP_001116137.1:n.1164+37del
NM_001302552.1:c.1155+37del	NP_001289481.1:n.1155+37del
NM_004660.4:c.1164+37del	NP_004651.2:n.1164+37del
XM_006724878.1:c.1164+37del	XP_006724941.1:n.1164+37del
XM_011531471.1:c.1164+37del	XP_011529773.1:n.1164+37del
NM_001122665.3:c.1164+37del	NP_001116137.1:n.1164+37del
NM_001302552.2:c.1155+37del	NP_001289481.1:n.1155+37del
NM_001324195.1:c.1164+37del	NP_001311124.1:n.1164+37del
NR_136716.1:n.1633+37del
NR_136717.1:n.1395+37del
NR_136718.1:n.1713+37del
NR_136719.1:n.1503+37del
NR_136720.1:n.1633+37del
NR_136721.1:n.1226+37del
NR_136722.1:n.1310+37del
NR_136723.1:n.1628+37del
NR_136724.1:n.1548+37del
XR_001756014.2:n.1268+37del
NM_004660.5:c.1164+37del MANE Select	NP_004651.2:n.1164+37del
NM_001302552.3:c.1155+37del	NP_001289481.1:n.1155+37del
NM_001324195.2:c.1164+37del	NP_001311124.1:n.1164+37del
NR_136716.2:n.1551+37del
NR_136717.2:n.1313+37del
NR_136718.2:n.1631+37del
NR_136719.2:n.1421+37del
NR_136720.2:n.1551+37del
NR_136721.2:n.1216+37del