Canonical Allele Identifier: CA414987356

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027596G>C (hg19) ; chrY:g.12915684G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915684G>C , CM000686.2:g.12915684G>C	GRCh38
NC_000024.9:g.15027596G>C , CM000686.1:g.15027596G>C	GRCh37
NC_000024.8:g.13536990G>C	NCBI36
NG_012831.1:g.16578G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1074G>C MANE Select	ENSP00000336725.3:p.Gln358His
ENST00000336079.7:c.1074G>C	ENSP00000336725.3:p.Gln358His
ENST00000360160.8:c.1074G>C	ENSP00000353284.4:p.Gln358His
ENST00000495478.1:n.189G>C
NM_001122665.2:c.1074G>C	NP_001116137.1:p.Gln358His
NM_001302552.1:c.1065G>C	NP_001289481.1:p.Gln355His
NM_004660.4:c.1074G>C	NP_004651.2:p.Gln358His
XM_006724878.1:c.1074G>C	XP_006724941.1:p.Gln358His
XM_011531471.1:c.1074G>C	XP_011529773.1:p.Gln358His
NM_001122665.3:c.1074G>C	NP_001116137.1:p.Gln358His
NM_001302552.2:c.1065G>C	NP_001289481.1:p.Gln355His
NM_001324195.1:c.1074G>C	NP_001311124.1:p.Gln358His
NR_136716.1:n.1543G>C
NR_136717.1:n.1305G>C
NR_136718.1:n.1623G>C
NR_136719.1:n.1413G>C
NR_136720.1:n.1543G>C
NR_136721.1:n.1136G>C
NR_136722.1:n.1220G>C
NR_136723.1:n.1538G>C
NR_136724.1:n.1458G>C
XR_001756014.2:n.1178G>C
NM_004660.5:c.1074G>C MANE Select	NP_004651.2:p.Gln358His
NM_001302552.3:c.1065G>C	NP_001289481.1:p.Gln355His
NM_001324195.2:c.1074G>C	NP_001311124.1:p.Gln358His
NR_136716.2:n.1461G>C
NR_136717.2:n.1223G>C
NR_136718.2:n.1541G>C
NR_136719.2:n.1331G>C
NR_136720.2:n.1461G>C
NR_136721.2:n.1126G>C