Canonical Allele Identifier: CA2766243885

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918850T>C , CM000686.2:g.12918850T>C	GRCh38
NC_000024.9:g.15030762T>C , CM000686.1:g.15030762T>C	GRCh37
NC_000024.8:g.13540156T>C	NCBI36
NG_012831.1:g.19744T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*728T>C MANE Select	ENSP00000336725.3:n.*728T>C
ENST00000336079.7:c.*728T>C	ENSP00000336725.3:n.*728T>C
NM_004660.4:c.*728T>C	NP_004651.2:n.*728T>C
XM_006724878.1:c.*728T>C	XP_006724941.1:n.*728T>C
NM_001122665.3:c.*728T>C	NP_001116137.1:n.*728T>C
NM_001302552.2:c.*728T>C	NP_001289481.1:n.*728T>C
NM_001324195.1:c.*728T>C	NP_001311124.1:n.*728T>C
NR_136716.1:n.3180T>C
NR_136717.1:n.2942T>C
NR_136718.1:n.3260T>C
NR_136719.1:n.3050T>C
NR_136720.1:n.3111T>C
NR_136721.1:n.2773T>C
NR_136722.1:n.2857T>C
NR_136723.1:n.3175T>C
NR_136724.1:n.3095T>C
XR_001756014.2:n.2875T>C
NM_004660.5:c.*728T>C MANE Select	NP_004651.2:n.*728T>C
NM_001302552.3:c.*728T>C	NP_001289481.1:n.*728T>C
NM_001324195.2:c.*728T>C	NP_001311124.1:n.*728T>C
NR_136716.2:n.3098T>C
NR_136717.2:n.2860T>C
NR_136718.2:n.3178T>C
NR_136719.2:n.2968T>C
NR_136720.2:n.3029T>C
NR_136721.2:n.2763T>C