Canonical Allele Identifier: CA2470565268

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918770C= , CM000686.2:g.12918770C=	GRCh38
NC_000024.9:g.15030682C= , CM000686.1:g.15030682C=	GRCh37
NC_000024.8:g.13540076C=	NCBI36
NG_012831.1:g.19664C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.*648C= MANE Select	ENSP00000336725.3:n.*648C=
ENST00000336079.7:c.*648C=	ENSP00000336725.3:n.*648C=
NM_004660.4:c.*648C=	NP_004651.2:n.*648C=
XM_006724878.1:c.*648C=	XP_006724941.1:n.*648C=
NM_001122665.3:c.*648C=	NP_001116137.1:n.*648C=
NM_001302552.2:c.*648C=	NP_001289481.1:n.*648C=
NM_001324195.1:c.*648C=	NP_001311124.1:n.*648C=
NR_136716.1:n.3100C=
NR_136717.1:n.2862C=
NR_136718.1:n.3180C=
NR_136719.1:n.2970C=
NR_136720.1:n.3031C=
NR_136721.1:n.2693C=
NR_136722.1:n.2777C=
NR_136723.1:n.3095C=
NR_136724.1:n.3015C=
XR_001756014.2:n.2795C=
NM_004660.5:c.*648C= MANE Select	NP_004651.2:n.*648C=
NM_001302552.3:c.*648C=	NP_001289481.1:n.*648C=
NM_001324195.2:c.*648C=	NP_001311124.1:n.*648C=
NR_136716.2:n.3018C=
NR_136717.2:n.2780C=
NR_136718.2:n.3098C=
NR_136719.2:n.2888C=
NR_136720.2:n.2949C=
NR_136721.2:n.2683C=