Canonical Allele Identifier: CA414987845

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027681A>G (hg19) ; chrY:g.12915769A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915769A>G , CM000686.2:g.12915769A>G	GRCh38
NC_000024.9:g.15027681A>G , CM000686.1:g.15027681A>G	GRCh37
NC_000024.8:g.13537075A>G	NCBI36
NG_012831.1:g.16663A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1159A>G MANE Select	ENSP00000336725.3:p.Ile387Val
ENST00000336079.7:c.1159A>G	ENSP00000336725.3:p.Ile387Val
ENST00000360160.8:c.1159A>G	ENSP00000353284.4:p.Ile387Val
ENST00000495478.1:n.274A>G
NM_001122665.2:c.1159A>G	NP_001116137.1:p.Ile387Val
NM_001302552.1:c.1150A>G	NP_001289481.1:p.Ile384Val
NM_004660.4:c.1159A>G	NP_004651.2:p.Ile387Val
XM_006724878.1:c.1159A>G	XP_006724941.1:p.Ile387Val
XM_011531471.1:c.1159A>G	XP_011529773.1:p.Ile387Val
NM_001122665.3:c.1159A>G	NP_001116137.1:p.Ile387Val
NM_001302552.2:c.1150A>G	NP_001289481.1:p.Ile384Val
NM_001324195.1:c.1159A>G	NP_001311124.1:p.Ile387Val
NR_136716.1:n.1628A>G
NR_136717.1:n.1390A>G
NR_136718.1:n.1708A>G
NR_136719.1:n.1498A>G
NR_136720.1:n.1628A>G
NR_136721.1:n.1221A>G
NR_136722.1:n.1305A>G
NR_136723.1:n.1623A>G
NR_136724.1:n.1543A>G
XR_001756014.2:n.1263A>G
NM_004660.5:c.1159A>G MANE Select	NP_004651.2:p.Ile387Val
NM_001302552.3:c.1150A>G	NP_001289481.1:p.Ile384Val
NM_001324195.2:c.1159A>G	NP_001311124.1:p.Ile387Val
NR_136716.2:n.1546A>G
NR_136717.2:n.1308A>G
NR_136718.2:n.1626A>G
NR_136719.2:n.1416A>G
NR_136720.2:n.1546A>G
NR_136721.2:n.1211A>G