Canonical Allele Identifier: CA2766243442

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914783A>C , CM000686.2:g.12914783A>C	GRCh38
NC_000024.9:g.15026695A>C , CM000686.1:g.15026695A>C	GRCh37
NC_000024.8:g.13536089A>C	NCBI36
NG_012831.1:g.15677A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.760-101A>C MANE Select	ENSP00000336725.3:n.760-101A>C
ENST00000336079.7:c.760-101A>C	ENSP00000336725.3:n.760-101A>C
ENST00000360160.8:c.760-101A>C	ENSP00000353284.4:n.760-101A>C
ENST00000463199.1:n.278-101A>C
ENST00000472510.5:n.456A>C
NM_001122665.2:c.760-101A>C	NP_001116137.1:n.760-101A>C
NM_001302552.1:c.751-101A>C	NP_001289481.1:n.751-101A>C
NM_004660.4:c.760-101A>C	NP_004651.2:n.760-101A>C
XM_006724878.1:c.760-101A>C	XP_006724941.1:n.760-101A>C
XM_011531471.1:c.760-101A>C	XP_011529773.1:n.760-101A>C
NM_001122665.3:c.760-101A>C	NP_001116137.1:n.760-101A>C
NM_001302552.2:c.751-101A>C	NP_001289481.1:n.751-101A>C
NM_001324195.1:c.760-101A>C	NP_001311124.1:n.760-101A>C
NR_136716.1:n.1044A>C
NR_136717.1:n.991-101A>C
NR_136718.1:n.1124A>C
NR_136719.1:n.914A>C
NR_136720.1:n.1044A>C
NR_136721.1:n.839-101A>C
NR_136722.1:n.906-101A>C
NR_136723.1:n.1039A>C
NR_136724.1:n.959A>C
XR_001756014.2:n.864-101A>C
NM_004660.5:c.760-101A>C MANE Select	NP_004651.2:n.760-101A>C
NM_001302552.3:c.751-101A>C	NP_001289481.1:n.751-101A>C
NM_001324195.2:c.760-101A>C	NP_001311124.1:n.760-101A>C
NR_136716.2:n.962A>C
NR_136717.2:n.909-101A>C
NR_136718.2:n.1042A>C
NR_136719.2:n.832A>C
NR_136720.2:n.962A>C
NR_136721.2:n.829-101A>C