Canonical Allele Identifier: CA414983387

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15025654A>C (hg19) ; chrY:g.12913742A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12913742A>C , CM000686.2:g.12913742A>C	GRCh38
NC_000024.9:g.15025654A>C , CM000686.1:g.15025654A>C	GRCh37
NC_000024.8:g.13535048A>C	NCBI36
NG_012831.1:g.14636A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.562A>C MANE Select	ENSP00000336725.3:p.Ile188Leu
ENST00000336079.7:c.562A>C	ENSP00000336725.3:p.Ile188Leu
ENST00000360160.8:c.562A>C	ENSP00000353284.4:p.Ile188Leu
ENST00000440554.1:c.553A>C	ENSP00000400377.1:p.Ile185Leu
ENST00000454054.5:c.562A>C	ENSP00000398953.1:p.Ile188Leu
ENST00000463199.1:n.80A>C
ENST00000469101.1:n.448A>C
ENST00000472510.5:n.125A>C
NM_001122665.2:c.562A>C	NP_001116137.1:p.Ile188Leu
NM_001302552.1:c.553A>C	NP_001289481.1:p.Ile185Leu
NM_004660.4:c.562A>C	NP_004651.2:p.Ile188Leu
XM_006724878.1:c.562A>C	XP_006724941.1:p.Ile188Leu
XM_011531471.1:c.562A>C	XP_011529773.1:p.Ile188Leu
NM_001122665.3:c.562A>C	NP_001116137.1:p.Ile188Leu
NM_001302552.2:c.553A>C	NP_001289481.1:p.Ile185Leu
NM_001324195.1:c.562A>C	NP_001311124.1:p.Ile188Leu
NR_136716.1:n.713A>C
NR_136717.1:n.793A>C
NR_136718.1:n.793A>C
NR_136719.1:n.583A>C
NR_136720.1:n.713A>C
NR_136721.1:n.641A>C
NR_136722.1:n.708A>C
NR_136723.1:n.708A>C
NR_136724.1:n.628A>C
XR_001756014.2:n.666A>C
NM_004660.5:c.562A>C MANE Select	NP_004651.2:p.Ile188Leu
NM_001302552.3:c.553A>C	NP_001289481.1:p.Ile185Leu
NM_001324195.2:c.562A>C	NP_001311124.1:p.Ile188Leu
NR_136716.2:n.631A>C
NR_136717.2:n.711A>C
NR_136718.2:n.711A>C
NR_136719.2:n.501A>C
NR_136720.2:n.631A>C
NR_136721.2:n.631A>C