Canonical Allele Identifier: CA414987375

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027599A>G (hg19) ; chrY:g.12915687A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915687A>G , CM000686.2:g.12915687A>G	GRCh38
NC_000024.9:g.15027599A>G , CM000686.1:g.15027599A>G	GRCh37
NC_000024.8:g.13536993A>G	NCBI36
NG_012831.1:g.16581A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1077A>G MANE Select	ENSP00000336725.3:p.Ile359Met
ENST00000336079.7:c.1077A>G	ENSP00000336725.3:p.Ile359Met
ENST00000360160.8:c.1077A>G	ENSP00000353284.4:p.Ile359Met
ENST00000495478.1:n.192A>G
NM_001122665.2:c.1077A>G	NP_001116137.1:p.Ile359Met
NM_001302552.1:c.1068A>G	NP_001289481.1:p.Ile356Met
NM_004660.4:c.1077A>G	NP_004651.2:p.Ile359Met
XM_006724878.1:c.1077A>G	XP_006724941.1:p.Ile359Met
XM_011531471.1:c.1077A>G	XP_011529773.1:p.Ile359Met
NM_001122665.3:c.1077A>G	NP_001116137.1:p.Ile359Met
NM_001302552.2:c.1068A>G	NP_001289481.1:p.Ile356Met
NM_001324195.1:c.1077A>G	NP_001311124.1:p.Ile359Met
NR_136716.1:n.1546A>G
NR_136717.1:n.1308A>G
NR_136718.1:n.1626A>G
NR_136719.1:n.1416A>G
NR_136720.1:n.1546A>G
NR_136721.1:n.1139A>G
NR_136722.1:n.1223A>G
NR_136723.1:n.1541A>G
NR_136724.1:n.1461A>G
XR_001756014.2:n.1181A>G
NM_004660.5:c.1077A>G MANE Select	NP_004651.2:p.Ile359Met
NM_001302552.3:c.1068A>G	NP_001289481.1:p.Ile356Met
NM_001324195.2:c.1077A>G	NP_001311124.1:p.Ile359Met
NR_136716.2:n.1464A>G
NR_136717.2:n.1226A>G
NR_136718.2:n.1544A>G
NR_136719.2:n.1334A>G
NR_136720.2:n.1464A>G
NR_136721.2:n.1129A>G