Canonical Allele Identifier: CA414987133

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027558G>C (hg19) ; chrY:g.12915646G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915646G>C , CM000686.2:g.12915646G>C	GRCh38
NC_000024.9:g.15027558G>C , CM000686.1:g.15027558G>C	GRCh37
NC_000024.8:g.13536952G>C	NCBI36
NG_012831.1:g.16540G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.1036G>C MANE Select	ENSP00000336725.3:p.Glu346Gln
ENST00000336079.7:c.1036G>C	ENSP00000336725.3:p.Glu346Gln
ENST00000360160.8:c.1036G>C	ENSP00000353284.4:p.Glu346Gln
ENST00000495478.1:n.151G>C
NM_001122665.2:c.1036G>C	NP_001116137.1:p.Glu346Gln
NM_001302552.1:c.1027G>C	NP_001289481.1:p.Glu343Gln
NM_004660.4:c.1036G>C	NP_004651.2:p.Glu346Gln
XM_006724878.1:c.1036G>C	XP_006724941.1:p.Glu346Gln
XM_011531471.1:c.1036G>C	XP_011529773.1:p.Glu346Gln
NM_001122665.3:c.1036G>C	NP_001116137.1:p.Glu346Gln
NM_001302552.2:c.1027G>C	NP_001289481.1:p.Glu343Gln
NM_001324195.1:c.1036G>C	NP_001311124.1:p.Glu346Gln
NR_136716.1:n.1505G>C
NR_136717.1:n.1267G>C
NR_136718.1:n.1585G>C
NR_136719.1:n.1375G>C
NR_136720.1:n.1505G>C
NR_136721.1:n.1098G>C
NR_136722.1:n.1182G>C
NR_136723.1:n.1500G>C
NR_136724.1:n.1420G>C
XR_001756014.2:n.1140G>C
NM_004660.5:c.1036G>C MANE Select	NP_004651.2:p.Glu346Gln
NM_001302552.3:c.1027G>C	NP_001289481.1:p.Glu343Gln
NM_001324195.2:c.1036G>C	NP_001311124.1:p.Glu346Gln
NR_136716.2:n.1423G>C
NR_136717.2:n.1185G>C
NR_136718.2:n.1503G>C
NR_136719.2:n.1293G>C
NR_136720.2:n.1423G>C
NR_136721.2:n.1088G>C