Canonical Allele Identifier: CA2766243418

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914665T>C , CM000686.2:g.12914665T>C	GRCh38
NC_000024.9:g.15026577T>C , CM000686.1:g.15026577T>C	GRCh37
NC_000024.8:g.13535971T>C	NCBI36
NG_012831.1:g.15559T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.759+16T>C MANE Select	ENSP00000336725.3:n.759+16T>C
ENST00000336079.7:c.759+16T>C	ENSP00000336725.3:n.759+16T>C
ENST00000360160.8:c.759+16T>C	ENSP00000353284.4:n.759+16T>C
ENST00000463199.1:n.277+16T>C
ENST00000472510.5:n.338T>C
NM_001122665.2:c.759+16T>C	NP_001116137.1:n.759+16T>C
NM_001302552.1:c.750+16T>C	NP_001289481.1:n.750+16T>C
NM_004660.4:c.759+16T>C	NP_004651.2:n.759+16T>C
XM_006724878.1:c.759+16T>C	XP_006724941.1:n.759+16T>C
XM_011531471.1:c.759+16T>C	XP_011529773.1:n.759+16T>C
NM_001122665.3:c.759+16T>C	NP_001116137.1:n.759+16T>C
NM_001302552.2:c.750+16T>C	NP_001289481.1:n.750+16T>C
NM_001324195.1:c.759+16T>C	NP_001311124.1:n.759+16T>C
NR_136716.1:n.926T>C
NR_136717.1:n.990+16T>C
NR_136718.1:n.1006T>C
NR_136719.1:n.796T>C
NR_136720.1:n.926T>C
NR_136721.1:n.838+16T>C
NR_136722.1:n.905+16T>C
NR_136723.1:n.921T>C
NR_136724.1:n.841T>C
XR_001756014.2:n.863+16T>C
NM_004660.5:c.759+16T>C MANE Select	NP_004651.2:n.759+16T>C
NM_001302552.3:c.750+16T>C	NP_001289481.1:n.750+16T>C
NM_001324195.2:c.759+16T>C	NP_001311124.1:n.759+16T>C
NR_136716.2:n.844T>C
NR_136717.2:n.908+16T>C
NR_136718.2:n.924T>C
NR_136719.2:n.714T>C
NR_136720.2:n.844T>C
NR_136721.2:n.828+16T>C