Canonical Allele Identifier: CA519905803

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029405C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917493C>T , CM000686.2:g.12917493C>T	GRCh38
NC_000024.9:g.15029405C>T , CM000686.1:g.15029405C>T	GRCh37
NC_000024.8:g.13538799C>T	NCBI36
NG_012831.1:g.18387C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1854C>T MANE Select	ENSP00000336725.3:p.Ser618=
ENST00000336079.7:c.1854C>T	ENSP00000336725.3:p.Ser618=
ENST00000360160.8:c.1854C>T	ENSP00000353284.4:p.Ser618=
NM_001122665.2:c.1854C>T	NP_001116137.1:p.Ser618=
NM_001302552.1:c.1845C>T	NP_001289481.1:p.Ser615=
NM_004660.4:c.1854C>T	NP_004651.2:p.Ser618=
XM_006724878.1:c.1785C>T	XP_006724941.1:p.Ser595=
NM_001122665.3:c.1854C>T	NP_001116137.1:p.Ser618=
NM_001302552.2:c.1845C>T	NP_001289481.1:p.Ser615=
NM_001324195.1:c.1785C>T	NP_001311124.1:p.Ser595=
NR_136716.1:n.2323C>T
NR_136717.1:n.2085C>T
NR_136718.1:n.2403C>T
NR_136719.1:n.2193C>T
NR_136720.1:n.2254C>T
NR_136721.1:n.1916C>T
NR_136722.1:n.2000C>T
NR_136723.1:n.2318C>T
NR_136724.1:n.2238C>T
XR_001756014.2:n.2018C>T
NM_004660.5:c.1854C>T MANE Select	NP_004651.2:p.Ser618=
NM_001302552.3:c.1845C>T	NP_001289481.1:p.Ser615=
NM_001324195.2:c.1785C>T	NP_001311124.1:p.Ser595=
NR_136716.2:n.2241C>T
NR_136717.2:n.2003C>T
NR_136718.2:n.2321C>T
NR_136719.2:n.2111C>T
NR_136720.2:n.2172C>T
NR_136721.2:n.1906C>T