Canonical Allele Identifier: CA2470564360

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12905642A= , CM000686.2:g.12905642A=	GRCh38
NC_000024.9:g.15017553A= , CM000686.1:g.15017553A=	GRCh37
NC_000024.8:g.13526947A=	NCBI36
NG_012831.1:g.6535A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.45+661A= MANE Select	ENSP00000336725.3:n.45+661A=
ENST00000336079.7:c.45+661A=	ENSP00000336725.3:n.45+661A=
ENST00000360160.8:c.45+661A=	ENSP00000353284.4:n.45+661A=
ENST00000454054.5:c.45+661A=	ENSP00000398953.1:n.45+661A=
ENST00000493363.1:n.133+661A=
NM_001122665.2:c.45+661A=	NP_001116137.1:n.45+661A=
NM_004660.4:c.45+661A=	NP_004651.2:n.45+661A=
XM_006724878.1:c.45+661A=	XP_006724941.1:n.45+661A=
XM_011531471.1:c.45+661A=	XP_011529773.1:n.45+661A=
NM_001122665.3:c.45+661A=	NP_001116137.1:n.45+661A=
NM_001324195.1:c.45+661A=	NP_001311124.1:n.45+661A=
NR_136716.1:n.196+661A=
NR_136717.1:n.196+661A=
NR_136718.1:n.196+661A=
NR_136719.1:n.196+661A=
NR_136720.1:n.196+661A=
NR_136721.1:n.124+661A=
XR_001756014.2:n.149+661A=
NM_004660.5:c.45+661A= MANE Select	NP_004651.2:n.45+661A=
NM_001324195.2:c.45+661A=	NP_001311124.1:n.45+661A=
NR_136716.2:n.114+661A=
NR_136717.2:n.114+661A=
NR_136718.2:n.114+661A=
NR_136719.2:n.114+661A=
NR_136720.2:n.114+661A=
NR_136721.2:n.114+661A=