Canonical Allele Identifier: CA1139171422

Gene: DDX3Y

Linked Data

• dbSNP Id: rs2053658221
• gnomAD v3: Y-12918695-T-G
• gnomAD v4: Y-12918695-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918695T>G , CM000686.2:g.12918695T>G	GRCh38
NC_000024.9:g.15030607T>G , CM000686.1:g.15030607T>G	GRCh37
NC_000024.8:g.13540001T>G	NCBI36
NG_012831.1:g.19589T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.*573T>G MANE Select	ENSP00000336725.3:n.*573T>G
ENST00000336079.7:c.*573T>G	ENSP00000336725.3:n.*573T>G
NM_004660.4:c.*573T>G	NP_004651.2:n.*573T>G
XM_006724878.1:c.*573T>G	XP_006724941.1:n.*573T>G
NM_001122665.3:c.*573T>G	NP_001116137.1:n.*573T>G
NM_001302552.2:c.*573T>G	NP_001289481.1:n.*573T>G
NM_001324195.1:c.*573T>G	NP_001311124.1:n.*573T>G
NR_136716.1:n.3025T>G
NR_136717.1:n.2787T>G
NR_136718.1:n.3105T>G
NR_136719.1:n.2895T>G
NR_136720.1:n.2956T>G
NR_136721.1:n.2618T>G
NR_136722.1:n.2702T>G
NR_136723.1:n.3020T>G
NR_136724.1:n.2940T>G
XR_001756014.2:n.2720T>G
NM_004660.5:c.*573T>G MANE Select	NP_004651.2:n.*573T>G
NM_001302552.3:c.*573T>G	NP_001289481.1:n.*573T>G
NM_001324195.2:c.*573T>G	NP_001311124.1:n.*573T>G
NR_136716.2:n.2943T>G
NR_136717.2:n.2705T>G
NR_136718.2:n.3023T>G
NR_136719.2:n.2813T>G
NR_136720.2:n.2874T>G
NR_136721.2:n.2608T>G