Canonical Allele Identifier: CA414987650

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027648A>T (hg19) ; chrY:g.12915736A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915736A>T , CM000686.2:g.12915736A>T	GRCh38
NC_000024.9:g.15027648A>T , CM000686.1:g.15027648A>T	GRCh37
NC_000024.8:g.13537042A>T	NCBI36
NG_012831.1:g.16630A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1126A>T MANE Select	ENSP00000336725.3:p.Thr376Ser
ENST00000336079.7:c.1126A>T	ENSP00000336725.3:p.Thr376Ser
ENST00000360160.8:c.1126A>T	ENSP00000353284.4:p.Thr376Ser
ENST00000495478.1:n.241A>T
NM_001122665.2:c.1126A>T	NP_001116137.1:p.Thr376Ser
NM_001302552.1:c.1117A>T	NP_001289481.1:p.Thr373Ser
NM_004660.4:c.1126A>T	NP_004651.2:p.Thr376Ser
XM_006724878.1:c.1126A>T	XP_006724941.1:p.Thr376Ser
XM_011531471.1:c.1126A>T	XP_011529773.1:p.Thr376Ser
NM_001122665.3:c.1126A>T	NP_001116137.1:p.Thr376Ser
NM_001302552.2:c.1117A>T	NP_001289481.1:p.Thr373Ser
NM_001324195.1:c.1126A>T	NP_001311124.1:p.Thr376Ser
NR_136716.1:n.1595A>T
NR_136717.1:n.1357A>T
NR_136718.1:n.1675A>T
NR_136719.1:n.1465A>T
NR_136720.1:n.1595A>T
NR_136721.1:n.1188A>T
NR_136722.1:n.1272A>T
NR_136723.1:n.1590A>T
NR_136724.1:n.1510A>T
XR_001756014.2:n.1230A>T
NM_004660.5:c.1126A>T MANE Select	NP_004651.2:p.Thr376Ser
NM_001302552.3:c.1117A>T	NP_001289481.1:p.Thr373Ser
NM_001324195.2:c.1126A>T	NP_001311124.1:p.Thr376Ser
NR_136716.2:n.1513A>T
NR_136717.2:n.1275A>T
NR_136718.2:n.1593A>T
NR_136719.2:n.1383A>T
NR_136720.2:n.1513A>T
NR_136721.2:n.1178A>T