Canonical Allele Identifier: CA2470565041

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915753T= , CM000686.2:g.12915753T=	GRCh38
NC_000024.9:g.15027665T= , CM000686.1:g.15027665T=	GRCh37
NC_000024.8:g.13537059T=	NCBI36
NG_012831.1:g.16647T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1143T= MANE Select	ENSP00000336725.3:p.Ala381=
ENST00000336079.7:c.1143T=	ENSP00000336725.3:p.Ala381=
ENST00000360160.8:c.1143T=	ENSP00000353284.4:p.Ala381=
ENST00000495478.1:n.258T=
NM_001122665.2:c.1143T=	NP_001116137.1:p.Ala381=
NM_001302552.1:c.1134T=	NP_001289481.1:p.Ala378=
NM_004660.4:c.1143T=	NP_004651.2:p.Ala381=
XM_006724878.1:c.1143T=	XP_006724941.1:p.Ala381=
XM_011531471.1:c.1143T=	XP_011529773.1:p.Ala381=
NM_001122665.3:c.1143T=	NP_001116137.1:p.Ala381=
NM_001302552.2:c.1134T=	NP_001289481.1:p.Ala378=
NM_001324195.1:c.1143T=	NP_001311124.1:p.Ala381=
NR_136716.1:n.1612T=
NR_136717.1:n.1374T=
NR_136718.1:n.1692T=
NR_136719.1:n.1482T=
NR_136720.1:n.1612T=
NR_136721.1:n.1205T=
NR_136722.1:n.1289T=
NR_136723.1:n.1607T=
NR_136724.1:n.1527T=
XR_001756014.2:n.1247T=
NM_004660.5:c.1143T= MANE Select	NP_004651.2:p.Ala381=
NM_001302552.3:c.1134T=	NP_001289481.1:p.Ala378=
NM_001324195.2:c.1143T=	NP_001311124.1:p.Ala381=
NR_136716.2:n.1530T=
NR_136717.2:n.1292T=
NR_136718.2:n.1610T=
NR_136719.2:n.1400T=
NR_136720.2:n.1530T=
NR_136721.2:n.1195T=