Canonical Allele Identifier: CA519896093

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15025683C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12913771C>G , CM000686.2:g.12913771C>G	GRCh38
NC_000024.9:g.15025683C>G , CM000686.1:g.15025683C>G	GRCh37
NC_000024.8:g.13535077C>G	NCBI36
NG_012831.1:g.14665C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.591C>G MANE Select	ENSP00000336725.3:p.Arg197=
ENST00000336079.7:c.591C>G	ENSP00000336725.3:p.Arg197=
ENST00000360160.8:c.591C>G	ENSP00000353284.4:p.Arg197=
ENST00000440554.1:c.582C>G	ENSP00000400377.1:p.Arg194=
ENST00000454054.5:c.591C>G	ENSP00000398953.1:p.Arg197=
ENST00000463199.1:n.109C>G
ENST00000469101.1:n.477C>G
ENST00000472510.5:n.154C>G
NM_001122665.2:c.591C>G	NP_001116137.1:p.Arg197=
NM_001302552.1:c.582C>G	NP_001289481.1:p.Arg194=
NM_004660.4:c.591C>G	NP_004651.2:p.Arg197=
XM_006724878.1:c.591C>G	XP_006724941.1:p.Arg197=
XM_011531471.1:c.591C>G	XP_011529773.1:p.Arg197=
NM_001122665.3:c.591C>G	NP_001116137.1:p.Arg197=
NM_001302552.2:c.582C>G	NP_001289481.1:p.Arg194=
NM_001324195.1:c.591C>G	NP_001311124.1:p.Arg197=
NR_136716.1:n.742C>G
NR_136717.1:n.822C>G
NR_136718.1:n.822C>G
NR_136719.1:n.612C>G
NR_136720.1:n.742C>G
NR_136721.1:n.670C>G
NR_136722.1:n.737C>G
NR_136723.1:n.737C>G
NR_136724.1:n.657C>G
XR_001756014.2:n.695C>G
NM_004660.5:c.591C>G MANE Select	NP_004651.2:p.Arg197=
NM_001302552.3:c.582C>G	NP_001289481.1:p.Arg194=
NM_001324195.2:c.591C>G	NP_001311124.1:p.Arg197=
NR_136716.2:n.660C>G
NR_136717.2:n.740C>G
NR_136718.2:n.740C>G
NR_136719.2:n.530C>G
NR_136720.2:n.660C>G
NR_136721.2:n.660C>G