Canonical Allele Identifier: CA414992640

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029394C>G (hg19) ; chrY:g.12917482C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917482C>G , CM000686.2:g.12917482C>G	GRCh38
NC_000024.9:g.15029394C>G , CM000686.1:g.15029394C>G	GRCh37
NC_000024.8:g.13538788C>G	NCBI36
NG_012831.1:g.18376C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1843C>G MANE Select	ENSP00000336725.3:p.Arg615Gly
ENST00000336079.7:c.1843C>G	ENSP00000336725.3:p.Arg615Gly
ENST00000360160.8:c.1843C>G	ENSP00000353284.4:p.Arg615Gly
NM_001122665.2:c.1843C>G	NP_001116137.1:p.Arg615Gly
NM_001302552.1:c.1834C>G	NP_001289481.1:p.Arg612Gly
NM_004660.4:c.1843C>G	NP_004651.2:p.Arg615Gly
XM_006724878.1:c.1774C>G	XP_006724941.1:p.Arg592Gly
NM_001122665.3:c.1843C>G	NP_001116137.1:p.Arg615Gly
NM_001302552.2:c.1834C>G	NP_001289481.1:p.Arg612Gly
NM_001324195.1:c.1774C>G	NP_001311124.1:p.Arg592Gly
NR_136716.1:n.2312C>G
NR_136717.1:n.2074C>G
NR_136718.1:n.2392C>G
NR_136719.1:n.2182C>G
NR_136720.1:n.2243C>G
NR_136721.1:n.1905C>G
NR_136722.1:n.1989C>G
NR_136723.1:n.2307C>G
NR_136724.1:n.2227C>G
XR_001756014.2:n.2007C>G
NM_004660.5:c.1843C>G MANE Select	NP_004651.2:p.Arg615Gly
NM_001302552.3:c.1834C>G	NP_001289481.1:p.Arg612Gly
NM_001324195.2:c.1774C>G	NP_001311124.1:p.Arg592Gly
NR_136716.2:n.2230C>G
NR_136717.2:n.1992C>G
NR_136718.2:n.2310C>G
NR_136719.2:n.2100C>G
NR_136720.2:n.2161C>G
NR_136721.2:n.1895C>G