Canonical Allele Identifier: CA2470565174

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917501G= , CM000686.2:g.12917501G=	GRCh38
NC_000024.9:g.15029413G= , CM000686.1:g.15029413G=	GRCh37
NC_000024.8:g.13538807G=	NCBI36
NG_012831.1:g.18395G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1862G= MANE Select	ENSP00000336725.3:p.Ser621=
ENST00000336079.7:c.1862G=	ENSP00000336725.3:p.Ser621=
ENST00000360160.8:c.1862G=	ENSP00000353284.4:p.Ser621=
NM_001122665.2:c.1862G=	NP_001116137.1:p.Ser621=
NM_001302552.1:c.1853G=	NP_001289481.1:p.Ser618=
NM_004660.4:c.1862G=	NP_004651.2:p.Ser621=
XM_006724878.1:c.1793G=	XP_006724941.1:p.Ser598=
NM_001122665.3:c.1862G=	NP_001116137.1:p.Ser621=
NM_001302552.2:c.1853G=	NP_001289481.1:p.Ser618=
NM_001324195.1:c.1793G=	NP_001311124.1:p.Ser598=
NR_136716.1:n.2331G=
NR_136717.1:n.2093G=
NR_136718.1:n.2411G=
NR_136719.1:n.2201G=
NR_136720.1:n.2262G=
NR_136721.1:n.1924G=
NR_136722.1:n.2008G=
NR_136723.1:n.2326G=
NR_136724.1:n.2246G=
XR_001756014.2:n.2026G=
NM_004660.5:c.1862G= MANE Select	NP_004651.2:p.Ser621=
NM_001302552.3:c.1853G=	NP_001289481.1:p.Ser618=
NM_001324195.2:c.1793G=	NP_001311124.1:p.Ser598=
NR_136716.2:n.2249G=
NR_136717.2:n.2011G=
NR_136718.2:n.2329G=
NR_136719.2:n.2119G=
NR_136720.2:n.2180G=
NR_136721.2:n.1914G=