Canonical Allele Identifier: CA337722326

Gene: DDX3Y

Linked Data

• dbSNP Id: rs550257571
• MyVariant Identifiers: chrY:g.15030664T>C (hg19) ; chrY:g.12918752T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918752T>C , CM000686.2:g.12918752T>C	GRCh38
NC_000024.9:g.15030664T>C , CM000686.1:g.15030664T>C	GRCh37
NC_000024.8:g.13540058T>C	NCBI36
NG_012831.1:g.19646T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*630T>C MANE Select	ENSP00000336725.3:n.*630T>C
ENST00000336079.7:c.*630T>C	ENSP00000336725.3:n.*630T>C
NM_004660.4:c.*630T>C	NP_004651.2:n.*630T>C
XM_006724878.1:c.*630T>C	XP_006724941.1:n.*630T>C
NM_001122665.3:c.*630T>C	NP_001116137.1:n.*630T>C
NM_001302552.2:c.*630T>C	NP_001289481.1:n.*630T>C
NM_001324195.1:c.*630T>C	NP_001311124.1:n.*630T>C
NR_136716.1:n.3082T>C
NR_136717.1:n.2844T>C
NR_136718.1:n.3162T>C
NR_136719.1:n.2952T>C
NR_136720.1:n.3013T>C
NR_136721.1:n.2675T>C
NR_136722.1:n.2759T>C
NR_136723.1:n.3077T>C
NR_136724.1:n.2997T>C
XR_001756014.2:n.2777T>C
NM_004660.5:c.*630T>C MANE Select	NP_004651.2:n.*630T>C
NM_001302552.3:c.*630T>C	NP_001289481.1:n.*630T>C
NM_001324195.2:c.*630T>C	NP_001311124.1:n.*630T>C
NR_136716.2:n.3000T>C
NR_136717.2:n.2762T>C
NR_136718.2:n.3080T>C
NR_136719.2:n.2870T>C
NR_136720.2:n.2931T>C
NR_136721.2:n.2665T>C