Canonical Allele Identifier: CA414983293

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15025634G>C (hg19) ; chrY:g.12913722G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12913722G>C , CM000686.2:g.12913722G>C	GRCh38
NC_000024.9:g.15025634G>C , CM000686.1:g.15025634G>C	GRCh37
NC_000024.8:g.13535028G>C	NCBI36
NG_012831.1:g.14616G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.542G>C MANE Select	ENSP00000336725.3:p.Ser181Thr
ENST00000336079.7:c.542G>C	ENSP00000336725.3:p.Ser181Thr
ENST00000360160.8:c.542G>C	ENSP00000353284.4:p.Ser181Thr
ENST00000440554.1:c.533G>C	ENSP00000400377.1:p.Ser178Thr
ENST00000454054.5:c.542G>C	ENSP00000398953.1:p.Ser181Thr
ENST00000463199.1:n.60G>C
ENST00000469101.1:n.428G>C
ENST00000472510.5:n.105G>C
NM_001122665.2:c.542G>C	NP_001116137.1:p.Ser181Thr
NM_001302552.1:c.533G>C	NP_001289481.1:p.Ser178Thr
NM_004660.4:c.542G>C	NP_004651.2:p.Ser181Thr
XM_006724878.1:c.542G>C	XP_006724941.1:p.Ser181Thr
XM_011531471.1:c.542G>C	XP_011529773.1:p.Ser181Thr
NM_001122665.3:c.542G>C	NP_001116137.1:p.Ser181Thr
NM_001302552.2:c.533G>C	NP_001289481.1:p.Ser178Thr
NM_001324195.1:c.542G>C	NP_001311124.1:p.Ser181Thr
NR_136716.1:n.693G>C
NR_136717.1:n.773G>C
NR_136718.1:n.773G>C
NR_136719.1:n.563G>C
NR_136720.1:n.693G>C
NR_136721.1:n.621G>C
NR_136722.1:n.688G>C
NR_136723.1:n.688G>C
NR_136724.1:n.608G>C
XR_001756014.2:n.646G>C
NM_004660.5:c.542G>C MANE Select	NP_004651.2:p.Ser181Thr
NM_001302552.3:c.533G>C	NP_001289481.1:p.Ser178Thr
NM_001324195.2:c.542G>C	NP_001311124.1:p.Ser181Thr
NR_136716.2:n.611G>C
NR_136717.2:n.691G>C
NR_136718.2:n.691G>C
NR_136719.2:n.481G>C
NR_136720.2:n.611G>C
NR_136721.2:n.611G>C