Canonical Allele Identifier: CA2509877544

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918679A>G , CM000686.2:g.12918679A>G	GRCh38
NC_000024.9:g.15030591A>G , CM000686.1:g.15030591A>G	GRCh37
NC_000024.8:g.13539985A>G	NCBI36
NG_012831.1:g.19573A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*557A>G MANE Select	ENSP00000336725.3:n.*557A>G
ENST00000336079.7:c.*557A>G	ENSP00000336725.3:n.*557A>G
NM_004660.4:c.*557A>G	NP_004651.2:n.*557A>G
XM_006724878.1:c.*557A>G	XP_006724941.1:n.*557A>G
NM_001122665.3:c.*557A>G	NP_001116137.1:n.*557A>G
NM_001302552.2:c.*557A>G	NP_001289481.1:n.*557A>G
NM_001324195.1:c.*557A>G	NP_001311124.1:n.*557A>G
NR_136716.1:n.3009A>G
NR_136717.1:n.2771A>G
NR_136718.1:n.3089A>G
NR_136719.1:n.2879A>G
NR_136720.1:n.2940A>G
NR_136721.1:n.2602A>G
NR_136722.1:n.2686A>G
NR_136723.1:n.3004A>G
NR_136724.1:n.2924A>G
XR_001756014.2:n.2704A>G
NM_004660.5:c.*557A>G MANE Select	NP_004651.2:n.*557A>G
NM_001302552.3:c.*557A>G	NP_001289481.1:n.*557A>G
NM_001324195.2:c.*557A>G	NP_001311124.1:n.*557A>G
NR_136716.2:n.2927A>G
NR_136717.2:n.2689A>G
NR_136718.2:n.3007A>G
NR_136719.2:n.2797A>G
NR_136720.2:n.2858A>G
NR_136721.2:n.2592A>G