Canonical Allele Identifier: CA414987413

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027607T>G (hg19) ; chrY:g.12915695T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915695T>G , CM000686.2:g.12915695T>G	GRCh38
NC_000024.9:g.15027607T>G , CM000686.1:g.15027607T>G	GRCh37
NC_000024.8:g.13537001T>G	NCBI36
NG_012831.1:g.16589T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1085T>G MANE Select	ENSP00000336725.3:p.Ile362Arg
ENST00000336079.7:c.1085T>G	ENSP00000336725.3:p.Ile362Arg
ENST00000360160.8:c.1085T>G	ENSP00000353284.4:p.Ile362Arg
ENST00000495478.1:n.200T>G
NM_001122665.2:c.1085T>G	NP_001116137.1:p.Ile362Arg
NM_001302552.1:c.1076T>G	NP_001289481.1:p.Ile359Arg
NM_004660.4:c.1085T>G	NP_004651.2:p.Ile362Arg
XM_006724878.1:c.1085T>G	XP_006724941.1:p.Ile362Arg
XM_011531471.1:c.1085T>G	XP_011529773.1:p.Ile362Arg
NM_001122665.3:c.1085T>G	NP_001116137.1:p.Ile362Arg
NM_001302552.2:c.1076T>G	NP_001289481.1:p.Ile359Arg
NM_001324195.1:c.1085T>G	NP_001311124.1:p.Ile362Arg
NR_136716.1:n.1554T>G
NR_136717.1:n.1316T>G
NR_136718.1:n.1634T>G
NR_136719.1:n.1424T>G
NR_136720.1:n.1554T>G
NR_136721.1:n.1147T>G
NR_136722.1:n.1231T>G
NR_136723.1:n.1549T>G
NR_136724.1:n.1469T>G
XR_001756014.2:n.1189T>G
NM_004660.5:c.1085T>G MANE Select	NP_004651.2:p.Ile362Arg
NM_001302552.3:c.1076T>G	NP_001289481.1:p.Ile359Arg
NM_001324195.2:c.1085T>G	NP_001311124.1:p.Ile362Arg
NR_136716.2:n.1472T>G
NR_136717.2:n.1234T>G
NR_136718.2:n.1552T>G
NR_136719.2:n.1342T>G
NR_136720.2:n.1472T>G
NR_136721.2:n.1137T>G