Canonical Allele Identifier: CA2824889396

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914691A>G , CM000686.2:g.12914691A>G	GRCh38
NC_000024.9:g.15026603A>G , CM000686.1:g.15026603A>G	GRCh37
NC_000024.8:g.13535997A>G	NCBI36
NG_012831.1:g.15585A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.759+42A>G MANE Select	ENSP00000336725.3:n.759+42A>G
ENST00000336079.7:c.759+42A>G	ENSP00000336725.3:n.759+42A>G
ENST00000360160.8:c.759+42A>G	ENSP00000353284.4:n.759+42A>G
ENST00000463199.1:n.277+42A>G
ENST00000472510.5:n.364A>G
NM_001122665.2:c.759+42A>G	NP_001116137.1:n.759+42A>G
NM_001302552.1:c.750+42A>G	NP_001289481.1:n.750+42A>G
NM_004660.4:c.759+42A>G	NP_004651.2:n.759+42A>G
XM_006724878.1:c.759+42A>G	XP_006724941.1:n.759+42A>G
XM_011531471.1:c.759+42A>G	XP_011529773.1:n.759+42A>G
NM_001122665.3:c.759+42A>G	NP_001116137.1:n.759+42A>G
NM_001302552.2:c.750+42A>G	NP_001289481.1:n.750+42A>G
NM_001324195.1:c.759+42A>G	NP_001311124.1:n.759+42A>G
NR_136716.1:n.952A>G
NR_136717.1:n.990+42A>G
NR_136718.1:n.1032A>G
NR_136719.1:n.822A>G
NR_136720.1:n.952A>G
NR_136721.1:n.838+42A>G
NR_136722.1:n.905+42A>G
NR_136723.1:n.947A>G
NR_136724.1:n.867A>G
XR_001756014.2:n.863+42A>G
NM_004660.5:c.759+42A>G MANE Select	NP_004651.2:n.759+42A>G
NM_001302552.3:c.750+42A>G	NP_001289481.1:n.750+42A>G
NM_001324195.2:c.759+42A>G	NP_001311124.1:n.759+42A>G
NR_136716.2:n.870A>G
NR_136717.2:n.908+42A>G
NR_136718.2:n.950A>G
NR_136719.2:n.740A>G
NR_136720.2:n.870A>G
NR_136721.2:n.828+42A>G