Canonical Allele Identifier: CA2535614322

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918797G>C , CM000686.2:g.12918797G>C	GRCh38
NC_000024.9:g.15030709G>C , CM000686.1:g.15030709G>C	GRCh37
NC_000024.8:g.13540103G>C	NCBI36
NG_012831.1:g.19691G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*675G>C MANE Select	ENSP00000336725.3:n.*675G>C
ENST00000336079.7:c.*675G>C	ENSP00000336725.3:n.*675G>C
NM_004660.4:c.*675G>C	NP_004651.2:n.*675G>C
XM_006724878.1:c.*675G>C	XP_006724941.1:n.*675G>C
NM_001122665.3:c.*675G>C	NP_001116137.1:n.*675G>C
NM_001302552.2:c.*675G>C	NP_001289481.1:n.*675G>C
NM_001324195.1:c.*675G>C	NP_001311124.1:n.*675G>C
NR_136716.1:n.3127G>C
NR_136717.1:n.2889G>C
NR_136718.1:n.3207G>C
NR_136719.1:n.2997G>C
NR_136720.1:n.3058G>C
NR_136721.1:n.2720G>C
NR_136722.1:n.2804G>C
NR_136723.1:n.3122G>C
NR_136724.1:n.3042G>C
XR_001756014.2:n.2822G>C
NM_004660.5:c.*675G>C MANE Select	NP_004651.2:n.*675G>C
NM_001302552.3:c.*675G>C	NP_001289481.1:n.*675G>C
NM_001324195.2:c.*675G>C	NP_001311124.1:n.*675G>C
NR_136716.2:n.3045G>C
NR_136717.2:n.2807G>C
NR_136718.2:n.3125G>C
NR_136719.2:n.2915G>C
NR_136720.2:n.2976G>C
NR_136721.2:n.2710G>C