Canonical Allele Identifier: CA414984760

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026541G>C (hg19) ; chrY:g.12914629G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914629G>C , CM000686.2:g.12914629G>C	GRCh38
NC_000024.9:g.15026541G>C , CM000686.1:g.15026541G>C	GRCh37
NC_000024.8:g.13535935G>C	NCBI36
NG_012831.1:g.15523G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.739G>C MANE Select	ENSP00000336725.3:p.Glu247Gln
ENST00000336079.7:c.739G>C	ENSP00000336725.3:p.Glu247Gln
ENST00000360160.8:c.739G>C	ENSP00000353284.4:p.Glu247Gln
ENST00000440554.1:c.730G>C	ENSP00000400377.1:p.Glu244Gln
ENST00000463199.1:n.257G>C
ENST00000472510.5:n.302G>C
NM_001122665.2:c.739G>C	NP_001116137.1:p.Glu247Gln
NM_001302552.1:c.730G>C	NP_001289481.1:p.Glu244Gln
NM_004660.4:c.739G>C	NP_004651.2:p.Glu247Gln
XM_006724878.1:c.739G>C	XP_006724941.1:p.Glu247Gln
XM_011531471.1:c.739G>C	XP_011529773.1:p.Glu247Gln
NM_001122665.3:c.739G>C	NP_001116137.1:p.Glu247Gln
NM_001302552.2:c.730G>C	NP_001289481.1:p.Glu244Gln
NM_001324195.1:c.739G>C	NP_001311124.1:p.Glu247Gln
NR_136716.1:n.890G>C
NR_136717.1:n.970G>C
NR_136718.1:n.970G>C
NR_136719.1:n.760G>C
NR_136720.1:n.890G>C
NR_136721.1:n.818G>C
NR_136722.1:n.885G>C
NR_136723.1:n.885G>C
NR_136724.1:n.805G>C
XR_001756014.2:n.843G>C
NM_004660.5:c.739G>C MANE Select	NP_004651.2:p.Glu247Gln
NM_001302552.3:c.730G>C	NP_001289481.1:p.Glu244Gln
NM_001324195.2:c.739G>C	NP_001311124.1:p.Glu247Gln
NR_136716.2:n.808G>C
NR_136717.2:n.888G>C
NR_136718.2:n.888G>C
NR_136719.2:n.678G>C
NR_136720.2:n.808G>C
NR_136721.2:n.808G>C