Canonical Allele Identifier: CA2555263816

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918862C>A , CM000686.2:g.12918862C>A	GRCh38
NC_000024.9:g.15030774C>A , CM000686.1:g.15030774C>A	GRCh37
NC_000024.8:g.13540168C>A	NCBI36
NG_012831.1:g.19756C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.*740C>A MANE Select	ENSP00000336725.3:n.*740C>A
ENST00000336079.7:c.*740C>A	ENSP00000336725.3:n.*740C>A
NM_004660.4:c.*740C>A	NP_004651.2:n.*740C>A
XM_006724878.1:c.*740C>A	XP_006724941.1:n.*740C>A
NM_001122665.3:c.*740C>A	NP_001116137.1:n.*740C>A
NM_001302552.2:c.*740C>A	NP_001289481.1:n.*740C>A
NM_001324195.1:c.*740C>A	NP_001311124.1:n.*740C>A
NR_136716.1:n.3192C>A
NR_136717.1:n.2954C>A
NR_136718.1:n.3272C>A
NR_136719.1:n.3062C>A
NR_136720.1:n.3123C>A
NR_136721.1:n.2785C>A
NR_136722.1:n.2869C>A
NR_136723.1:n.3187C>A
NR_136724.1:n.3107C>A
XR_001756014.2:n.2887C>A
NM_004660.5:c.*740C>A MANE Select	NP_004651.2:n.*740C>A
NM_001302552.3:c.*740C>A	NP_001289481.1:n.*740C>A
NM_001324195.2:c.*740C>A	NP_001311124.1:n.*740C>A
NR_136716.2:n.3110C>A
NR_136717.2:n.2872C>A
NR_136718.2:n.3190C>A
NR_136719.2:n.2980C>A
NR_136720.2:n.3041C>A
NR_136721.2:n.2775C>A