Canonical Allele Identifier: CA414992716

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15029407G>A (hg19) ; chrY:g.12917495G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12917495G>A , CM000686.2:g.12917495G>A	GRCh38
NC_000024.9:g.15029407G>A , CM000686.1:g.15029407G>A	GRCh37
NC_000024.8:g.13538801G>A	NCBI36
NG_012831.1:g.18389G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1856G>A MANE Select	ENSP00000336725.3:p.Ser619Asn
ENST00000336079.7:c.1856G>A	ENSP00000336725.3:p.Ser619Asn
ENST00000360160.8:c.1856G>A	ENSP00000353284.4:p.Ser619Asn
NM_001122665.2:c.1856G>A	NP_001116137.1:p.Ser619Asn
NM_001302552.1:c.1847G>A	NP_001289481.1:p.Ser616Asn
NM_004660.4:c.1856G>A	NP_004651.2:p.Ser619Asn
XM_006724878.1:c.1787G>A	XP_006724941.1:p.Ser596Asn
NM_001122665.3:c.1856G>A	NP_001116137.1:p.Ser619Asn
NM_001302552.2:c.1847G>A	NP_001289481.1:p.Ser616Asn
NM_001324195.1:c.1787G>A	NP_001311124.1:p.Ser596Asn
NR_136716.1:n.2325G>A
NR_136717.1:n.2087G>A
NR_136718.1:n.2405G>A
NR_136719.1:n.2195G>A
NR_136720.1:n.2256G>A
NR_136721.1:n.1918G>A
NR_136722.1:n.2002G>A
NR_136723.1:n.2320G>A
NR_136724.1:n.2240G>A
XR_001756014.2:n.2020G>A
NM_004660.5:c.1856G>A MANE Select	NP_004651.2:p.Ser619Asn
NM_001302552.3:c.1847G>A	NP_001289481.1:p.Ser616Asn
NM_001324195.2:c.1787G>A	NP_001311124.1:p.Ser596Asn
NR_136716.2:n.2243G>A
NR_136717.2:n.2005G>A
NR_136718.2:n.2323G>A
NR_136719.2:n.2113G>A
NR_136720.2:n.2174G>A
NR_136721.2:n.1908G>A