Canonical Allele Identifier: CA414992675
Gene: DDX3Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12917489G>A , CM000686.2:g.12917489G>A GRCh38
NC_000024.9:g.15029401G>A , CM000686.1:g.15029401G>A GRCh37
NC_000024.8:g.13538795G>A NCBI36
NG_012831.1:g.18383G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.1850G>A MANE Select ENSP00000336725.3:p.Ser617Asn
ENST00000336079.7:c.1850G>A ENSP00000336725.3:p.Ser617Asn
ENST00000360160.8:c.1850G>A ENSP00000353284.4:p.Ser617Asn
NM_001122665.2:c.1850G>A NP_001116137.1:p.Ser617Asn
NM_001302552.1:c.1841G>A NP_001289481.1:p.Ser614Asn
NM_004660.4:c.1850G>A NP_004651.2:p.Ser617Asn
XM_006724878.1:c.1781G>A XP_006724941.1:p.Ser594Asn
NM_001122665.3:c.1850G>A NP_001116137.1:p.Ser617Asn
NM_001302552.2:c.1841G>A NP_001289481.1:p.Ser614Asn
NM_001324195.1:c.1781G>A NP_001311124.1:p.Ser594Asn
NR_136716.1:n.2319G>A
NR_136717.1:n.2081G>A
NR_136718.1:n.2399G>A
NR_136719.1:n.2189G>A
NR_136720.1:n.2250G>A
NR_136721.1:n.1912G>A
NR_136722.1:n.1996G>A
NR_136723.1:n.2314G>A
NR_136724.1:n.2234G>A
XR_001756014.2:n.2014G>A
NM_004660.5:c.1850G>A MANE Select NP_004651.2:p.Ser617Asn
NM_001302552.3:c.1841G>A NP_001289481.1:p.Ser614Asn
NM_001324195.2:c.1781G>A NP_001311124.1:p.Ser594Asn
NR_136716.2:n.2237G>A
NR_136717.2:n.1999G>A
NR_136718.2:n.2317G>A
NR_136719.2:n.2107G>A
NR_136720.2:n.2168G>A
NR_136721.2:n.1902G>A