Canonical Allele Identifier: CA414983576

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15025681C>A (hg19) ; chrY:g.12913769C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12913769C>A , CM000686.2:g.12913769C>A	GRCh38
NC_000024.9:g.15025681C>A , CM000686.1:g.15025681C>A	GRCh37
NC_000024.8:g.13535075C>A	NCBI36
NG_012831.1:g.14663C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.589C>A MANE Select	ENSP00000336725.3:p.Arg197Ser
ENST00000336079.7:c.589C>A	ENSP00000336725.3:p.Arg197Ser
ENST00000360160.8:c.589C>A	ENSP00000353284.4:p.Arg197Ser
ENST00000440554.1:c.580C>A	ENSP00000400377.1:p.Arg194Ser
ENST00000454054.5:c.589C>A	ENSP00000398953.1:p.Arg197Ser
ENST00000463199.1:n.107C>A
ENST00000469101.1:n.475C>A
ENST00000472510.5:n.152C>A
NM_001122665.2:c.589C>A	NP_001116137.1:p.Arg197Ser
NM_001302552.1:c.580C>A	NP_001289481.1:p.Arg194Ser
NM_004660.4:c.589C>A	NP_004651.2:p.Arg197Ser
XM_006724878.1:c.589C>A	XP_006724941.1:p.Arg197Ser
XM_011531471.1:c.589C>A	XP_011529773.1:p.Arg197Ser
NM_001122665.3:c.589C>A	NP_001116137.1:p.Arg197Ser
NM_001302552.2:c.580C>A	NP_001289481.1:p.Arg194Ser
NM_001324195.1:c.589C>A	NP_001311124.1:p.Arg197Ser
NR_136716.1:n.740C>A
NR_136717.1:n.820C>A
NR_136718.1:n.820C>A
NR_136719.1:n.610C>A
NR_136720.1:n.740C>A
NR_136721.1:n.668C>A
NR_136722.1:n.735C>A
NR_136723.1:n.735C>A
NR_136724.1:n.655C>A
XR_001756014.2:n.693C>A
NM_004660.5:c.589C>A MANE Select	NP_004651.2:p.Arg197Ser
NM_001302552.3:c.580C>A	NP_001289481.1:p.Arg194Ser
NM_001324195.2:c.589C>A	NP_001311124.1:p.Arg197Ser
NR_136716.2:n.658C>A
NR_136717.2:n.738C>A
NR_136718.2:n.738C>A
NR_136719.2:n.528C>A
NR_136720.2:n.658C>A
NR_136721.2:n.658C>A