Canonical Allele Identifier: CA414984385

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026493G>T (hg19) ; chrY:g.12914581G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914581G>T , CM000686.2:g.12914581G>T	GRCh38
NC_000024.9:g.15026493G>T , CM000686.1:g.15026493G>T	GRCh37
NC_000024.8:g.13535887G>T	NCBI36
NG_012831.1:g.15475G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.691G>T MANE Select	ENSP00000336725.3:p.Ala231Ser
ENST00000336079.7:c.691G>T	ENSP00000336725.3:p.Ala231Ser
ENST00000360160.8:c.691G>T	ENSP00000353284.4:p.Ala231Ser
ENST00000440554.1:c.682G>T	ENSP00000400377.1:p.Ala228Ser
ENST00000463199.1:n.209G>T
ENST00000472510.5:n.254G>T
NM_001122665.2:c.691G>T	NP_001116137.1:p.Ala231Ser
NM_001302552.1:c.682G>T	NP_001289481.1:p.Ala228Ser
NM_004660.4:c.691G>T	NP_004651.2:p.Ala231Ser
XM_006724878.1:c.691G>T	XP_006724941.1:p.Ala231Ser
XM_011531471.1:c.691G>T	XP_011529773.1:p.Ala231Ser
NM_001122665.3:c.691G>T	NP_001116137.1:p.Ala231Ser
NM_001302552.2:c.682G>T	NP_001289481.1:p.Ala228Ser
NM_001324195.1:c.691G>T	NP_001311124.1:p.Ala231Ser
NR_136716.1:n.842G>T
NR_136717.1:n.922G>T
NR_136718.1:n.922G>T
NR_136719.1:n.712G>T
NR_136720.1:n.842G>T
NR_136721.1:n.770G>T
NR_136722.1:n.837G>T
NR_136723.1:n.837G>T
NR_136724.1:n.757G>T
XR_001756014.2:n.795G>T
NM_004660.5:c.691G>T MANE Select	NP_004651.2:p.Ala231Ser
NM_001302552.3:c.682G>T	NP_001289481.1:p.Ala228Ser
NM_001324195.2:c.691G>T	NP_001311124.1:p.Ala231Ser
NR_136716.2:n.760G>T
NR_136717.2:n.840G>T
NR_136718.2:n.840G>T
NR_136719.2:n.630G>T
NR_136720.2:n.760G>T
NR_136721.2:n.760G>T