Canonical Allele Identifier: CA414992703

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029405C>G (hg19) ; chrY:g.12917493C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1854C>G MANE Select	ENSP00000336725.3:p.Ser618Arg
ENST00000336079.7:c.1854C>G	ENSP00000336725.3:p.Ser618Arg
ENST00000360160.8:c.1854C>G	ENSP00000353284.4:p.Ser618Arg
NM_001122665.2:c.1854C>G	NP_001116137.1:p.Ser618Arg
NM_001302552.1:c.1845C>G	NP_001289481.1:p.Ser615Arg
NM_004660.4:c.1854C>G	NP_004651.2:p.Ser618Arg
XM_006724878.1:c.1785C>G	XP_006724941.1:p.Ser595Arg
NM_001122665.3:c.1854C>G	NP_001116137.1:p.Ser618Arg
NM_001302552.2:c.1845C>G	NP_001289481.1:p.Ser615Arg
NM_001324195.1:c.1785C>G	NP_001311124.1:p.Ser595Arg
NR_136716.1:n.2323C>G
NR_136717.1:n.2085C>G
NR_136718.1:n.2403C>G
NR_136719.1:n.2193C>G
NR_136720.1:n.2254C>G
NR_136721.1:n.1916C>G
NR_136722.1:n.2000C>G
NR_136723.1:n.2318C>G
NR_136724.1:n.2238C>G
XR_001756014.2:n.2018C>G
NM_004660.5:c.1854C>G MANE Select	NP_004651.2:p.Ser618Arg
NM_001302552.3:c.1845C>G	NP_001289481.1:p.Ser615Arg
NM_001324195.2:c.1785C>G	NP_001311124.1:p.Ser595Arg
NR_136716.2:n.2241C>G
NR_136717.2:n.2003C>G
NR_136718.2:n.2321C>G
NR_136719.2:n.2111C>G
NR_136720.2:n.2172C>G
NR_136721.2:n.1906C>G