Canonical Allele Identifier: CA2766243879

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918746C>A , CM000686.2:g.12918746C>A	GRCh38
NC_000024.9:g.15030658C>A , CM000686.1:g.15030658C>A	GRCh37
NC_000024.8:g.13540052C>A	NCBI36
NG_012831.1:g.19640C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*624C>A MANE Select	ENSP00000336725.3:n.*624C>A
ENST00000336079.7:c.*624C>A	ENSP00000336725.3:n.*624C>A
NM_004660.4:c.*624C>A	NP_004651.2:n.*624C>A
XM_006724878.1:c.*624C>A	XP_006724941.1:n.*624C>A
NM_001122665.3:c.*624C>A	NP_001116137.1:n.*624C>A
NM_001302552.2:c.*624C>A	NP_001289481.1:n.*624C>A
NM_001324195.1:c.*624C>A	NP_001311124.1:n.*624C>A
NR_136716.1:n.3076C>A
NR_136717.1:n.2838C>A
NR_136718.1:n.3156C>A
NR_136719.1:n.2946C>A
NR_136720.1:n.3007C>A
NR_136721.1:n.2669C>A
NR_136722.1:n.2753C>A
NR_136723.1:n.3071C>A
NR_136724.1:n.2991C>A
XR_001756014.2:n.2771C>A
NM_004660.5:c.*624C>A MANE Select	NP_004651.2:n.*624C>A
NM_001302552.3:c.*624C>A	NP_001289481.1:n.*624C>A
NM_001324195.2:c.*624C>A	NP_001311124.1:n.*624C>A
NR_136716.2:n.2994C>A
NR_136717.2:n.2756C>A
NR_136718.2:n.3074C>A
NR_136719.2:n.2864C>A
NR_136720.2:n.2925C>A
NR_136721.2:n.2659C>A