Canonical Allele Identifier: CA2470565070

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12916264G= , CM000686.2:g.12916264G=	GRCh38
NC_000024.9:g.15028176G= , CM000686.1:g.15028176G=	GRCh37
NC_000024.8:g.13537570G=	NCBI36
NG_012831.1:g.17158G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004660.5:c.1313G= MANE Select	NP_004651.2:p.Ser438=
ENST00000336079.8:c.1313G= MANE Select	ENSP00000336725.3:p.Ser438=
NM_001122665.2:c.1313G=	NP_001116137.1:p.Ser438=
NM_001122665.3:c.1313G=	NP_001116137.1:p.Ser438=
NM_001302552.1:c.1304G=	NP_001289481.1:p.Ser435=
NM_001302552.2:c.1304G=	NP_001289481.1:p.Ser435=
NM_001302552.3:c.1304G=	NP_001289481.1:p.Ser435=
NM_001324195.1:c.1313G=	NP_001311124.1:p.Ser438=
NM_001324195.2:c.1313G=	NP_001311124.1:p.Ser438=
NM_004660.4:c.1313G=	NP_004651.2:p.Ser438=
NR_136716.1:n.1782G=
NR_136716.2:n.1700G=
NR_136717.1:n.1544G=
NR_136717.2:n.1462G=
NR_136718.1:n.1862G=
NR_136718.2:n.1780G=
NR_136719.1:n.1652G=
NR_136719.2:n.1570G=
NR_136720.1:n.1782G=
NR_136720.2:n.1700G=
NR_136721.1:n.1375G=
NR_136721.2:n.1365G=
NR_136722.1:n.1459G=
NR_136723.1:n.1777G=
NR_136724.1:n.1697G=
ENST00000336079.7:c.1313G=	ENSP00000336725.3:p.Ser438=
ENST00000360160.8:c.1313G=	ENSP00000353284.4:p.Ser438=
ENST00000495478.1:n.428G=
XM_006724878.1:c.1313G=	XP_006724941.1:p.Ser438=
XM_011531471.1:c.1313G=	XP_011529773.1:p.Ser438=
XR_001756014.2:n.1417G=